Where Innovations Meets Personalized and Precision Medicine

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Personalized and Precision Medicine Journal is an open-access access double-blind peer peer-reviewed publication which is published by AmitisGen TECH Dev Group, concerned with new concepts and findings in areas related to Personalized & Precision Medicine issues. PPMJ is a quarterly publication that welcomes original, review, novel, and high-impact articles in the journal's scope (See journal scope). PPMJ follows the Committee on Publication Ethics (COPE) and complies with the highest ethical standards in accordance with ethical laws. All submitted manuscripts are checked for similarity through a trustworthy software named iThenticate to be assured about its originality and then rigorously peer-reviewed by the reviewers.

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Nanoplatforms in Gastric Ulcer Therapy: A Narrative Review

Pages 1-8

https://doi.org/10.22034/ppmj.2026.2091019.1072

Mohammadreza Mohammad Hosseiniazar, Asad Hashemi

Abstract Introduction : Gastric ulcer is a common gastrointestinal disorder resulting from an imbalance between aggressive factors such as gastric acid, oxidative stress, chronic inflammation and protective mucosal mechanisms. Limitations of conventional therapies, including drug resistance, systemic side effects, and suboptimal efficacy in certain patients, underscore the need for novel therapeutic strategies. Nanoparticles, as advanced drug delivery systems, offer promising approaches for targeted gastric mucosal therapy by enhancing drug stability, enabling site-specific delivery, and minimizing adverse effects. This review aims to analyze the therapeutic applications of nanoplatforms in the management of gastric ulcers and associated infections.
Methods: A narrative review was conducted by systematically searching PubMed, Scopus, and Web of Science databases from 2010 to 2025. Standardized keywords included “gastric ulcer,” “nanoparticles,” “targeted drug delivery,” “Helicobacter pylori,” and “mucosal drug delivery systems.” Eligible studies comprised preclinical investigations, animal models, and relevant review articles. Data were extracted and analyzed qualitatively and thematically.
Results: The findings indicate that nanocarriers including poly (lactic-co-glycolic acid) (PLGA), chitosan, silver, gold, selenium nanoparticles, and plant-based formulations—enhance drug bioavailability, enable controlled release, improve mucoadhesion, and achieve targeted gastric delivery. These properties collectively facilitate accelerated mucosal healing and tissue regeneration. Key mechanisms include inhibition of inflammatory pathways such as NF-κB, reduction of pro-inflammatory cytokines (e.g., TNF-α, IL-6), attenuation of oxidative stress, enhancement of antioxidant defenses (SOD, CAT, NRF2), and antibacterial activity against H. pylori. Conversely, certain nanoparticles, such as titanium dioxide, may provoke local inflammation and mucosal injury, highlighting the importance of nanoparticle type and physicochemical properties.
Conclusion: Targeted nanoparticles, through controlled drug release, mucoadhesion, anti-inflammatory effects, and antibacterial activity, represent a novel and effective approach for gastric ulcer therapy However, heterogeneity in biological responses and potential toxicity necessitate further extensive preclinical studies and rigorously designed clinical trials to ensure the safety and efficacy of these nanomedicine strategies.

Personalized Phytotherapy of Brucellosis: Insights from Traditional Iranian Medicine

Pages 9-16

https://doi.org/10.22034/ppmj.2026.2087728.1071

MohamadReza Nazer, Masoumeh Tahmasebi, Mahmoud Bahmani

Abstract ABSTRACT
Brucellosis, a zoonotic disease caused by Brucella species, remains endemic in regions such as Iran and presents significant public health challenges. Conventional antibiotic therapies have limitations, including adverse effects and incomplete efficacy, which has led to growing interest in medicinal plants as complementary or alternative treatments. This study reviews Iranian medicinal plants with potential anti-brucellosis activity, examining their mechanisms based on both traditional knowledge and contemporary scientific research. A comprehensive literature search was conducted using keywords including "brucellosis," "Malta fever," "traditional medicine," "medicinal plants," and "treatment" in databases such as Google Scholar, SID, Magiran, and Scopus. Relevant articles were screened, and data were systematically extracted and analyzed to provide an integrative review. The analysis identified several medicinal plants with notable therapeutic potential against brucellosis, including Zingiber officinale Roscoe, Mentha piperita L., Cinnamomum verum J. Presl, Thymus vulgaris L., Salvia officinalis L., Origanum vulgare L., Matricaria chamomilla L., Aloe vera L., Cuminum cyminum L., Alcea rosea L., Achillea millefolium L., Calendula officinalis L., Allium cepa L., Anethum graveolens L., Apium graveolens L., Allium sativum L., Coriandrum sativum L., Cucurbita spp. L., Rosa canina L., Elaeagnus angustifolia L., Scrophularia deserti Eig, Berberis vulgaris L., Ziziphora tenuior L., and Alhagi maurorum Medik. Taxonomic analysis showed that the Lamiaceae family was most represented (24%), followed by Asteraceae and Apiaceae (16% each). Mechanistic analysis indicated that antibacterial activity accounted for 32% of therapeutic effects, followed by anti-inflammatory (24%) and antioxidant (20%) activities. Native Iranian medicinal plants may serve as effective complementary agents in the management of brucellosis. Their use, particularly in endemic regions, could enhance patients' quality of life and mitigate the side effects associated with conventional treatments. Nonetheless, further rigorous clinical studies are required to validate their efficacy and safety.

Exploratory Transcriptomic Profiling of Three RNA-Seq Samples Reveals Heterogeneity in KRAS-Associated Signaling and Epithelial Lineage Programs

Pages 17-25

https://doi.org/10.22034/ppmj.2026.738542

Negar Fallah Azad, Mohammad Sadegh Mahmoudvandyam

Abstract KRAS-driven lung adenocarcinoma is molecularly heterogeneous; however, evaluation of mutation-associated programs requires matched mutation and clinical metadata. Here, three GDC STAR-count RNA-sequencing files annotated with GENCODE v36 were analyzed to determine which transcriptomic conclusions could be supported from the available data alone. Protein-coding TPM values were used for library-level quality assessment, transcriptome-wide correlation, principal component analysis, sample-specific expression contrasts, and exploratory scoring of curated KRAS/MAPK, PI3K–AKT–mTOR, cell-cycle, epithelial-lineage, epithelial–mesenchymal transition, hypoxia, inflammatory, interferon, apoptosis, and NRF2-related gene sets. The samples contained 24.3–49.5 million assigned reads and 12,808–14,574 protein-coding genes with TPM ≥1. Pairwise transcriptome correlations ranged from r=0.745 to 0.825. Marked biological heterogeneity was observed. Sample 1 showed a secretory epithelial profile characterized by PAEP, CEACAM5, CEACAM6, BPIFA1, and EPCAM. Sample 2 displayed a keratinizing/squamous-like program dominated by KRT5, KRT6A, KRT14, KRT17, SPRR family genes, and elevated NRF2-associated and glycolytic scores. Sample 3 exhibited a strong alveolar-lineage and immune-associated profile, with high SFTPA1, SFTPA2, SFTPB, SFTPC, HLA-DRA, CD74, and inflammatory pathway scores. KRAS expression was detectable in all samples (16.33–30.09 TPM), but RNA expression alone could not establish KRAS mutation status. These findings demonstrate substantial lineage and pathway heterogeneity among the three transcriptomes and provide a hypothesis-generating framework for subsequent mutation-informed analysis. Mutation-stratified differential expression, prognostic modeling, and survival analysis were not performed because mutation and clinical outcome data were unavailable.

Beyond Dysbiosis: Multi-Omics, Personalized Interventions, and the Vaginal Microbiome in Female Reproductive Healt

Pages 26-43

https://doi.org/10.22034/ppmj.2026.738543

Hossein Mokhlesabadi Farahani, Yasin MokhlesabadiFarahani

Abstract The vaginal microbiome is a dynamic mucosal ecosystem that plays a crucial role in female reproductive health. Unlike the gut microbiome, where high diversity is often considered beneficial, a healthy vaginal microbiome in reproductive-age women is commonly recognized by low microbial diversity and dominance of Lactobacillus species, particularly Lactobacillus crispatus. These communities help maintain an acidic vaginal environment, inhibit pathogen growth, support epithelial barrier integrity, and regulate mucosal immune responses. Growing evidence links vaginal microbial composition and function to fertility, assisted reproductive technology outcomes, pregnancy complications, and gynecological disorders. Lactobacillus-dominant communities are generally associated with favorable reproductive outcomes, whereas high-diversity anaerobe-rich communities have been implicated in bacterial vaginosis, pelvic inflammatory disease, HPV persistence, cervical dysplasia, recurrent infections, preterm birth, and potentially impaired fertility. However, the traditional concept of dysbiosis is insufficient to explain the biological complexity of vaginal microbial ecosystems. Similar taxonomic profiles may differ in microbial gene content, metabolic activity, biofilm formation, inflammatory potential, ecological stability, and clinical impact. Therefore, multi-omics approaches, including metagenomics, metatranscriptomics, metabolomics, proteomics, and host-response profiling, provide a more comprehensive framework for understanding host–microbiome interactions. This review summarizes current evidence on the vaginal microbiome in fertility, pregnancy outcomes, and gynecological disorders, while emphasizing the transition from descriptive dysbiosis models toward functional, ecological, and personalized perspectives. Emerging strategies such as microbiome-based biomarkers, targeted probiotics, live biotherapeutics, vaginal microbiome transplantation, and AI-driven prediction models may support future precision gynecology. Nevertheless, clinical translation requires standardized methods, longitudinal studies, diverse cohorts, validated biomarkers, and careful ethical oversight.

Association of BRCA1 Founder Mutations (185delAG and 5382insC) and TNF-α -308 Polymorphism with Familial Breast Cancer in Iranian Women

Association of BRCA1 Founder Mutations (185delAG and 5382insC) and TNF-α -308 Polymorphism with Familial Breast Cancer in Iranian Women

Pages 44-53

https://doi.org/10.22034/ppmj.2026.738545

Zahra Bagheri, Sara Sanjarian, Masoud Houshmand, Hossein Rassi

Abstract Background:Breast cancer is one of the leading causes of cancer-related mortality among women worldwide. Germline mutations in the *BRCA1* gene and polymorphisms in the *TNF-α* gene have been implicated in breast cancer susceptibility. This study aimed to investigate the frequency of the *BRCA1* 185delAG and 5382insC mutations and their association with the *TNF-α* -308 G>A polymorphism for the early diagnosis of breast cancer in Iranian women.
Methods: A total of 84 archival breast tissue samples were collected from breast cancer patients treated at Khatam and Imam Khomeini hospitals. Genomic DNA was extracted using standard protocols. The *BRCA1* 185delAG and 5382insC mutations were analyzed by multiplex polymerase chain reaction (PCR), while the *TNF-α* -308 G>A polymorphism was determined using amplification refractory mutation system PCR (ARMS-PCR). Histopathological characteristics, including mitotic activity, necrosis, cellular pleomorphism, tumor grade, and the expression of ER, PR, and p53, were evaluated using standard histopathological and immunohistochemical methods. Statistical analysis was performed using the chi-square test in Epi Info version 7, with a significance level of *P* < 0.05.
Results: Among the 84 patients, 38 had a positive family history of breast cancer and 46 had no family history. In patients with a positive family history, three cases carried the *BRCA1* 5382insC mutation and two carried the 185delAG mutation, whereas only one 5382insC mutation was detected in patients without a family history. The distribution of *TNF-α* -308 genotypes (AA, AG, and GG) was 8, 14, and 16 cases, respectively, among patients with a family history, compared with 25, 12, and 9 cases in those without a family history. Conclusion: The findings suggest that the *BRCA1* 185delAG and 5382insC mutations, together with the *TNF-α* -308 GG genotype and clinicopathological characteristics, may serve as useful molecular markers for identifying women at increased risk of breast cancer. Their combined assessment may improve the early diagnosis and facilitate timely therapeutic intervention in Iranian women.

Circulating miR-21-5p as a Diagnostic Biomarker in Colorectal Cancer: Clinical Evaluation and Integrated Bioinformatics Analysis of Its Molecular Targets

Circulating miR-21-5p as a Diagnostic Biomarker in Colorectal Cancer: Clinical Evaluation and Integrated Bioinformatics Analysis of Its Molecular Targets

Pages 54-63

https://doi.org/10.22034/ppmj.2026.738541

Farnoosh Honarmand, Mahnaz Saremi

Abstract Background: Circulating microRNAs have emerged as promising minimally invasive biomarkers for colorectal cancer (CRC). This study evaluated the expression and diagnostic performance of circulating hsa-miR-21-5p and investigated its potential molecular targets using integrated bioinformatics analysis.
Methods: Plasma samples were obtained from 50 treatment-naïve male patients with histologically confirmed grade II CRC and 20 healthy male controls. Circulating RNA was extracted and miR-21-5p expression was quantified using stem-loop reverse transcription quantitative PCR. Hsa-miR-1228-3p was used as the endogenous reference, and relative expression was calculated using the 2^−ΔΔCq method. Diagnostic performance was assessed by receiver operating characteristic analysis. High-confidence target genes were identified using miRDB and TargetScan, followed by protein–protein interaction analysis using STRING.
Results: The mean ages of patients and controls were 55 and 49 years, respectively, with no significant between-group difference (P=0.162). Circulating miR-21-5p expression was significantly higher in CRC patients than in healthy controls (P=0.002). ROC analysis yielded an area under the curve of 0.873 (95% CI, 0.766–0.979; P<0.0001). Target prediction identified a set of high-confidence genes involved in cell proliferation, apoptosis, immune regulation, adhesion, extracellular-matrix organization, and transcriptional control. STRING analysis revealed a functionally connected network containing central signaling proteins, including STAT3, YAP1, SKP2, PDCD4, TRAF6, and SPRY-family proteins.
Conclusion: Circulating miR-21-5p demonstrated good ability to distinguish CRC patients from healthy controls. The bioinformatics findings suggest that its biological effects may involve interconnected oncogenic, apoptotic, immune, and invasion-related pathways.

The Multifaceted Role of CD154 in SLE: Pathogenesis, Receptor Interactions, and Emerging Therapies

Articles in Press, Accepted Manuscript, Available Online from 01 May 2025

https://doi.org/10.22034/pmj.2025.2058206.1058

Farnaz Eghbalpour, Farnaz Eghbalpour

Abstract Systemic lupus erythematosus (SLE) is a multifaceted autoimmune disorder characterized by immune dysregulation and multi-organ involvement. Central to its pathogenesis is the CD154/CD40 signaling axis, which orchestrates key immunological processes, including T-B cell collaboration, dendritic cell activation, and cytokine production. Recent findings have expanded the scope of CD154 beyond its classical receptor CD40, identifying integrins as alternative receptors, thus broadening its biological impact. These discoveries underline the complexity of CD154's role in SLE and its potential as a therapeutic target. First-generation CD154/CD40-targeted therapies showed promise but were hindered by thromboembolic complications. However, second-generation therapeutics, including monoclonal antibodies, small molecules, and gene-editing technologies, exhibit improved safety and efficacy profiles. This review delves into the molecular and cellular mechanisms of CD154 in SLE, explores its emerging roles through integrin interactions, and evaluates the therapeutic advancements targeting this axis. The findings highlight CD154 as a central mediator in SLE pathogenesis and a compelling target for innovative treatment strategies.

An Ethnographic Review of Medicinal Plants Used for Alleviating Menstrual Pain in the Western Border Ethnobotany of Iran

Articles in Press, Accepted Manuscript, Available Online from 01 May 2025

https://doi.org/10.22034/pmj.2025.2059289.1061

Alireza Soleimani Mamalo, Shabnam Vazifekhah

Abstract Introduction: In this context, the use of medicinal plants as a natural and effective remedy for relieving Menstrual pain has been acknowledged in the western border region of Iran, serving as an alternative or complementary therapeutic approach. The aim of this study is to identify the medicinal plants employed in this region of Iran for the treatment of menstrual pain.
Methodology: This review study employed keywords such as medicinal plants, Iran, menstrual pain, and the provinces of West Azerbaijan, East Azerbaijan, Ardabil, Kurdistan, Kermanshah, Ilam, Khuzestan, and their cities, along with ethnobotany terms. Databases such as Google Scholar, SID, MegaIran, PubMed, and Scopus were utilized for article searches. Ethnobotanical articles related to the topic were selected for text review.
Results: Based on the ethnobotanical review, it was identified that in the cities and provinces of the western border region of Iran, medicinal plants such as fennel, wild parsley, shepherd's purse, black cumin, thyme, dandelion, rue, safflower, myrtle, European hornbeam, Kurdistan pistachio, mint, marshmallow root, male orchid, yarrow, agrimony, nettle, bitter herb, verbena, horsetail, periwinkle, marigold, saffron, wild thyme, savory, rhubarb, and eastern chamomile are commonly used for managing, controlling, and treating menstrual pain. Notably, the highest diversity of plant species was observed in the regions of Behbahan, Khuzestan, and Zrewar, Kurdistan. Leaves were the most commonly used plant part, and the Asteraceae and Lamiaceae families presented the highest number of species, indicating the rich diversity of medicinal and traditional plant applications.
Conclusion: The findings of this study demonstrate that the local communities in the western border region of Iran possess extensive knowledge regarding the use of medicinal plants for alleviating menstrual pain. Documenting and scientifically exploring this knowledge could lay the groundwork for the development of effective and natural herbal medicines in the domain of women’s health.

The Use of Bacteriophages in Cancer Therapy

Articles in Press, Accepted Manuscript, Available Online from 28 October 2024

https://doi.org/10.22034/pmj.2024.2044427.1042

Sanaz Khosravi

Abstract Cancer is a catastrophic illness with a significant worldwide fatality rate, anticipated to rise in the next years. Contemporary treatment modalities, including chemotherapy and radiation therapy, include constraints such as adverse effects, inconsistent efficacy, elevated expenses, and restricted accessibility. Bacteriophages have arisen as multifaceted instruments in bioengineering, with significant promise in tissue engineering, vaccine formulation, and immunotherapy. Bacteriophages are being used extensively in several fields of biotechnology and medicine, with cancer treatment being the most compelling application. Numerous studies are increasingly validating the effectiveness and safety of phage-based vectors as systemic delivery vehicles for therapeutic genes and medicines in cancer treatment. Moreover, the genetic composition of phages may be used for the creation of innovative DNA vaccines and antigen display systems, since they provide a highly structured and repeated presentation of antigens to immune cells. Bacteriophages have created novel opportunities for the precise targeting of certain molecular determinants in cancer cells. Phages may serve as anticancer agents and as carriers for imaging compounds and medicines. This article introduces bacteriophage and examines the performance of bacteriophages and bacteriophage engineering in targeted cancer treatment.

The Role of Hormonal Therapy in the Management of Hormone Receptor-Positive Breast Cancer: Current Trends and Future Directions

Articles in Press, Accepted Manuscript, Available Online from 16 May 2026

https://doi.org/10.22034/pmj.2025.2050921.1052

Sahar Abareshi

Abstract Breast cancer is responsible for more than 2.3 million newly diagnosed cases each year, according to the statistics. A hormonal imbalance, which is defined by unregulated activity of estrogen and progesterone, is often the cause of this type of cancer. It has become easier to handle patients who have HR+ breast cancer, particularly in women who have both advanced and early-stage disease, as a result of the deployment of estrogen-blocking hormone treatment. The permissiveness of tamoxifen, which was the first selective estrogen receptor modulator (SERM) to be commercialized, made it possible for more hormonal therapies to be developed. The cornerstone of breast cancer treatment is comprised of aromatase inhibitors (AIs), selective estrogen receptor degraders (SERDs), and cyclin-dependent kinase inhibitors (CDK) 4/6. These three types of drugs ultimately lead to improved patient outcomes. On the other hand, the inherent or acquired resistance of cancers to hormone therapy continues to be a serious cause for concern. Alterations in the genetic makeup of the tumor, as well as the activation of alternate pathways, make this situation even worse. The increasing development of molecular biology, precision medicine, and targeted therapies, on the other hand, is pointing to a new strategy for dealing with these problems. The purpose of this study is to investigate prospective treatment options and to shed light on the significant role that hormone therapy plays in the management of HR-positive breast cancer.

Comparison of Hemodynamic Changes and Post-Anesthesia Pain Intensity in Premenopausal and Postmenopausal Women Undergoing Elective Abdominal Hysterectomy with General Anesthesia

Articles in Press, Accepted Manuscript, Available Online from 16 May 2026

https://doi.org/10.22034/ppmj.2026.2073252.1068

Hananeh Habib

Abstract Background: Menopause comes along with a set of hormonal and physiological changes that can change cardiovascular responses during surgeries, along with altering pain perception. This research intends to analyze pain intensity during and after anesthesia and changes in hemodynamics in pre- and post-menopausal women during elective abdominal hysterectomy under general anesthesia.
Methods: Elective surgery patients, in this case, were 88 in number, with each division having 44 patients (before menopause and after). Women in each group were defined as premenopausal (n=44) and postmenopausal (n=44) in equal proportion. Other metrics looked at were Systolic Blood Pressure (SBP) and Diastolic Blood Pressure (DBP), also known as SpO₂. Patients’ heart rate and SpO₂ were checked during the surgery and after the surgery as well. Pain was assessed with the use of standardized scale methods, and participants were questioned on the pain felt during the post-operative period.
Results: While the premenopause cohort showed lower fluctuations in sensitivity to changes in SBP, DBP, and HR during and after anesthesia, the Postmenopause cohort exhibited the opposite (p<0.05). In each group, the SpO₂ levels were maintained within normal limits and showed no significant group differences. In the postoperative period, the pain score was significantly higher in the postmenopausal group with lower pain tolerance and a higher requirement for analgesic treatment. Spoken demographics such as age, body mass index (BMI), and other associated conditions showed a moderating influence on the hemodynamic response and pain outcomes.
Conclusion: Following menopause, diminished vascular adaptability, along with increased sympathetic tone and decreased central pain modulatory control due to lack of estrogen, might explain the instability of hemodynamics and increased postoperative pain. These observations could help in the formulation of appropriate anaesthetic techniques and postoperative pain relief policies in relation to the reproductive status of women.

Polycystic ovary syndrome and genetic factors influencing its development: A review article

Polycystic ovary syndrome and genetic factors influencing its development: A review article

Volume 6, Issue 23, Autumn 2021, Pages 25-29

https://doi.org/10.22034/pmj.2021.249631

Tohid Piri-Gharaghie

Abstract Polycystic ovary syndrome (PCOS) is a common infertility disorder, affecting a significant proportion of the global population. This syndrome has been one of the most controversial entities in gynecological endocrinology for many years. Both genes and the environment contribute to PCOS. Obesity, exacerbated by poor dietary choices, and physical inactivity, worsens PCOS in susceptible individuals. PCOS is a complex and heterogeneous disorder characterized by hyperandrogenemia, hyperinsulinemia, insulin resistance, and chronic anovulation. Many candidate genes have been identified to be one of the causes of PCOS. Different studies have been carried out to find the genetic correlation of PCOS. It is essential to carry out such studies that identify the clear cause of PCOS and its genetic association and hormonal disbalance. Currently, PCOS is considered a polygenic trait that might result from the interaction of susceptible and protective genomic variants and environmental factors, during either prenatal or postnatal life.

Methylenetetrahydrofolate Reductase C677T (rs1801133) Polymorphism and Pemetrexed Treatment Outcome in Patients with Non–Small-Cell Lung Cancer

Methylenetetrahydrofolate Reductase C677T (rs1801133) Polymorphism and Pemetrexed Treatment Outcome in Patients with Non–Small-Cell Lung Cancer

Volume 6, Issue 23, Autumn 2021, Pages 5-9

https://doi.org/10.22034/pmj.2021.249035

Mohammad Hadi Abbasian, Nafiseh Ansarinejad, Tayeb Ramim, Farshid Fardad, Bahareh Abbasi

Abstract Background: Lung cancer is the first cause of cancer deaths in the world. Pemetrexed is an antifolate drug used as a first or second-line in the treatment of advanced non-small cell lung cancer (NSCLC) patients. Methylenetetrahydrofolate reductase (MTHFR) is an important enzyme in a folic acid metabolic pathway and a central role in clinical response to pemetrexed. The aim of this study was to investigate the association between rs1801133 polymorphism and the overall survival of metastatic NSCLC patients.  
Methods: Thirty-four patients with metastatic lung cancer were treated with pemetrexed-based regimen at Rasoul Akram Hospital, Tehran, Iran. Genomic DNA was extracted from the peripheral blood of patients before initiation of treatment. Genotyping of rs1801133 polymorphism was performed at the National Institute of Genetic Engineering by PCR-RFLP methods. Statistical analysis performed with SPSS software, version 21.0.
 Results: Thirty-four patients were enrolled in this study. 21 patients (62%) were male and 13 (38%) were female. The mean age of the patients was 58.90 years. rs1801133 polymorphism were not significantly associated with survival in patients treated with pemetrexed-based chemotherapy.
 Conclusion: Previous studies have demonstrated that MTHFR polymorphism may predict survival among pemetrexed-based regimen treated advanced non-squamous NSCLC patients. However, in this study, the examined polymorphisms were not associated with patients' survival.

Microplastic Neurotoxicity: Pathways, Mechanisms, and Implications for Neurodegenerative Disease

Microplastic Neurotoxicity: Pathways, Mechanisms, and Implications for Neurodegenerative Disease

Volume 10, Issue 37, Spring 2025, Pages 31-38

https://doi.org/10.22034/pmj.2025.2058727.1060

Shabnam Radbakhsh, Rezvan Norouzzadeh

Abstract This review synthesizes and elaborates on current studies examining the neurotoxic effects of microplastics, emphasizing their mechanisms of entry into the central nervous system and their possible involvement in the development of neurodegenerative disorders. The pervasive presence of microplastics in the environment has heightened concerns about their accumulation in biological systems, particularly their capacity to traverse biological boundaries and engage with neuronal tissues. This article seeks to synthesize and critically evaluate the existing scientific literature on microplastic neuroinvasion, concentrating on the mechanisms through which these particles penetrate the blood-brain barrier (BBB) specifically via transcellular, paracellular, or Trojan horse pathways—and their ensuing effects on neuronal homeostasis.

We investigate the physiological and molecular reactions triggered by microplastics, encompassing oxidative stress induction, mitochondrial failure, neuroinflammation, and synaptic disruption. These pathogenic processes may facilitate the onset and advancement of several neurodegenerative disorders, including Alzheimer’s disease, by intensifying amyloid-beta aggregation, tau phosphorylation, and neuroimmune activation. Additionally, we examine the burgeoning epidemiological and experimental evidence associating microplastic exposure with cognitive deterioration and neuronal impairment.

This review offers a thorough analysis of microplastic neurotoxicity by evaluating both in vitro and in vivo studies, with the objective of elucidating the potential neurological hazards associated with these environmental contaminants. We emphasize significant deficiencies in existing research and propose future avenues, encompassing enhanced detection techniques, public health initiatives, and efforts to reduce human exposure to microplastics.

Exploring the Attitudes, Beliefs and Perceptions of Undergraduate and Graduate Students in Bangladesh towards Precision Medicine and Pharmacogenomics Practice: A Qualitative Study

Exploring the Attitudes, Beliefs and Perceptions of Undergraduate and Graduate Students in Bangladesh towards Precision Medicine and Pharmacogenomics Practice: A Qualitative Study

Volume 8, Issue 29, Spring 2023, Pages 14-24

https://doi.org/10.22034/pmj.2023.705459

Nashrifa Israt Khanom, Saima Nur, Sheikh Sabrina Mustari, Omme Jamila, Abu Sa A Dat, Md Mehade Hasan, Mushfiquzzaman Mahim, Farhana Faiza Bristy, Nasrin Tamanna, Md.Moshrraf Hossen, Swapan Kumar Das, Tanvir Ahmed, Md. Ashrafuzzaman Sapon, Md. Shafiqul Islam, Md. Monirul Islam

Abstract The aim of this study is to investigate the attitude, beliefs, and perceptions among undergraduate and graduate students toward precession medicine (PM) and pharmacogenomics (PGx) practice. A cross-sectional survey is conducted amongst students from different universities in Bangladesh.The results of the survey showed that the majority of students had a positive attitude towards precision medicine and pharmacogenomics, perceiving it as a means to improve diagnosis and treatment accuracy. Furthermore, many students also expressed a willingness to learn more about precision medicine and pharmacogenomics, suggesting that there is potential for these practices to be utilized in Bangladesh. Particularly in this study, 337 students from life science and relevant programs participated. From this study, it is shown that 84% of graduate students and 74% of undergraduate students thought PM is a promising healthcare model. In addition, 39% of students are highly encouraged to pursue their post-graduation in the subject areas of PGx and PM to support patients. The majority (62%) thought that patient privacy was the ethical concern most closely related to pharmacogenomic testing, while 19% of respondents thought that data confidentiality was the key issue. The results provide insight into the potential of precision medicine and pharmacogenomics in Bangladesh and suggest that further research into the attitudes of healthcare professionals should be conducted in order to take full advantage of the potential of these practices.

Increased expression of the lnc H19 gene in the plasma of people with breast cancer

Increased expression of the lnc H19 gene in the plasma of people with breast cancer

Volume 5, Issue 17, Spring 2020, Pages 12-14

https://doi.org/10.22034/pmj.2020.43454

kazhaleh Mohammadi, Sadegh Shojaei Baghini, Mohammad Ali Saremi

Abstract The majority of ncRNAs are known as long non-coding RNAs (lncRNAs) whose length exceeds 200 nucleotides. H19, a lncRNA, is the transcription product of the H19 gene, an oncogene in breast cancer, and is highly expressed in cancer tissues compared with normal tissues. The expression level of H19 is associated with the oncogenesis, proliferation, invasion, metastasis, and drug resistance of breast cancer. H19 expression levels were detected in breast cancer plasma using qRT-Real-Time PCR assay in 50 breast cancer samples and 50 healthy control samples. The results showed that the expression of this gene in both the tissue and the plasma of patients increased compared to that of healthy individuals.

Comparison of different methods of DNA extraction from paraffin-embedded tissues

Comparison of different methods of DNA extraction from paraffin-embedded tissues

Volume 5, Issue 17, Spring 2020, Pages 5-8

https://doi.org/10.22034/pmj.2020.43452

Ramadhan Ibrahim, Saeed Megdadi, Sareh Bakhshandeh bavarsad, Najme Shojaei

Abstract The most common human archival specimens are formalin-fixed and paraffin-embedded tissues. PCR-based techniques have been coupled with new developments in the extraction of DNA from FFPE. Herein, we report the results of a comparison of different methods of DNA extraction from FFPE specimens, including phenol-chloroform, salting-out, and silica-based commercial kits. Results showed no significant differences between the amounts of DNA obtained from each of the extraction methods studied; however, the salting-out DNA extraction method described is much easier and less toxic than the phenol–chloroform method.

Analysis of EGFR gene mutations in tissue samples of lung cancer tumors

Analysis of EGFR gene mutations in tissue samples of lung cancer tumors

Volume 5, Issue 17, Spring 2020, Pages 1-4

https://doi.org/10.22034/pmj.2020.43451

Blnd Ibrahim Mohammed, Amir Mohammadi, Nafise Poorhasan

Abstract Lung cancer is the leading cause of cancer deaths worldwide. Approximately 25% of nonsmall-cell lung cancers have mutations in the EGFR gene, most of which occur in hotspot regions in exons 18, 19, 20, and 21. In-frame deletions in exon 19 (~50%) and the L858R point mutation in exon 21 (~40%) are associated with a favorable response to EGFR tyrosine kinase inhibitors. In this study, mutations of two exons of 19 and 21 in 50 lung cancer tumor samples were investigated by the sequence method. From 50 lung cancer patients, 8 (16%) patients had an L858R (c.2573T>G) mutation, 6 (12%) patients had deletion type 1a mutation, and one patient had deletion type 1b mutation. Examining the sequence of candidate genes associated with lung cancer can be very important in choosing the right treatment approach.

The Multifaceted Role of CD154 in SLE: Pathogenesis, Receptor Interactions, and Emerging Therapies

The Multifaceted Role of CD154 in SLE: Pathogenesis, Receptor Interactions, and Emerging Therapies

Articles in Press, Accepted Manuscript, Available Online from 01 May 2025

https://doi.org/10.22034/pmj.2025.2058206.1058

Farnaz Eghbalpour, Farnaz Eghbalpour

Abstract Systemic lupus erythematosus (SLE) is a multifaceted autoimmune disorder characterized by immune dysregulation and multi-organ involvement. Central to its pathogenesis is the CD154/CD40 signaling axis, which orchestrates key immunological processes, including T-B cell collaboration, dendritic cell activation, and cytokine production. Recent findings have expanded the scope of CD154 beyond its classical receptor CD40, identifying integrins as alternative receptors, thus broadening its biological impact. These discoveries underline the complexity of CD154's role in SLE and its potential as a therapeutic target. First-generation CD154/CD40-targeted therapies showed promise but were hindered by thromboembolic complications. However, second-generation therapeutics, including monoclonal antibodies, small molecules, and gene-editing technologies, exhibit improved safety and efficacy profiles. This review delves into the molecular and cellular mechanisms of CD154 in SLE, explores its emerging roles through integrin interactions, and evaluates the therapeutic advancements targeting this axis. The findings highlight CD154 as a central mediator in SLE pathogenesis and a compelling target for innovative treatment strategies.

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