{"title":"A strategic approach to genetic model selection in association studies: A practical guide.","authors":"Mostafa Saadat","doi":"10.22099/mbrc.2026.54476.2226","DOIUrl":"https://doi.org/10.22099/mbrc.2026.54476.2226","url":null,"abstract":"","PeriodicalId":19025,"journal":{"name":"Molecular Biology Research Communications","volume":"15 2","pages":"81-83"},"PeriodicalIF":1.0,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13148451/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147840578","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Artificial intelligence and genomic data privacy: Balancing innovation with security.","authors":"Leila Kohan","doi":"10.22099/mbrc.2025.54335.2217","DOIUrl":"10.22099/mbrc.2025.54335.2217","url":null,"abstract":"","PeriodicalId":19025,"journal":{"name":"Molecular Biology Research Communications","volume":"15 1","pages":"1-2"},"PeriodicalIF":1.0,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12673624/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145678335","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Juan David Bermudes-Contreras, Luis Manuel Arratia-Cortés, Maria Esther Ramírez-Moreno, Beatriz Zamora-López, Cesar López-Camarillo, Laurence A Marchat, Absalom Zamorano-Carrillo
{"title":"Molecular dynamics simulation of thermal activation of human TRPV1.","authors":"Juan David Bermudes-Contreras, Luis Manuel Arratia-Cortés, Maria Esther Ramírez-Moreno, Beatriz Zamora-López, Cesar López-Camarillo, Laurence A Marchat, Absalom Zamorano-Carrillo","doi":"10.22099/mbrc.2025.53301.2171","DOIUrl":"10.22099/mbrc.2025.53301.2171","url":null,"abstract":"<p><p>TRPV1 (Transient Receptor Potential Vanilloid 1) is a non-selective ion channel that responds to various thermal, chemical, mechanical, and ligand stimuli. It is expressed in various tissues, mainly in nociceptive neurons, adipocytes, and other cell types. This channel is involved in pain and temperature transition processes, although it has recently been implicated in adipocyte browning processes. That is why the study of this receptor has increased in recent years to understand the process of activation and inactivation by various stimuli. In this work, we focus on modeling a complete channel of human TRPV1 (hTRPV1), the structural changes, and especially the behavior of the pore when this protein is subjected to high temperatures (400 K). We report that when molecular dynamics simulate hTRPV1 at 400 K, it suffers an increase in the diameter of the two gates reported elsewhere in the pore, suggesting the opening of the channel. In this work, we describe the structural changes in the entire protein, concomitant to those in the pore, favoring this process, which might be associated with its biological activity.</p>","PeriodicalId":19025,"journal":{"name":"Molecular Biology Research Communications","volume":"15 1","pages":"39-48"},"PeriodicalIF":1.0,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12673628/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145677711","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Therapeutic potential of 4-OH-coumarin in neuroblastoma: cellular, molecular, and epigenetic insights.","authors":"Çağrı Öner, Halise Elif Kulakac, Damla Kolcuoğlu, Ertuğrul Çolak","doi":"10.22099/mbrc.2025.54532.2228","DOIUrl":"10.22099/mbrc.2025.54532.2228","url":null,"abstract":"<p><p>The effect of 4-OH-Coumarin, a warfarin derivate, on the cellular characteristics and metastasis of SH-SY5Y neuroblastoma cells and HUVEC cells was aimed to determine. After IC50 concentrations were detected wound healing and hematoxylin-eosin assays were performed on both cell lines. Ki-67, hTERT, PI3K, AKT, mTOR, HIF-1α, PINK1, Parkin, Cyt C, p53 gene expressions and piR-651, piR-823, miR-126 expressions were determined by RT-PCR. The proliferation, wound closure and survival decreased after 4-OH-Coumarin treatment (<i>p</i><0.001). Ki-67, hTERT, PI3K, mTOR, HIF-1α, PINK1, Parkin, Cyt C and piR-823 expressions were decreased, while AKT, p53, piR-651, and miR-126 increased on SH-SY5Y (<i>p</i><0.001). AKT (<i>p</i><0.05), Parkin, and piR-651 expressions increased on only HUVEC cells (p<0.001). We believe that the study of various molecules that are secondary metabolites such as 4-OH-Coumarin may provide valuable data to observe the effects and mechanisms of new therapeutics that have the potential to be used for cancer treatment.</p>","PeriodicalId":19025,"journal":{"name":"Molecular Biology Research Communications","volume":"15 2","pages":"103-116"},"PeriodicalIF":1.4,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13148452/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147840156","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Ahmad Reza Khosravi, Özlem Çetin, Atena Eslami-Farouji
{"title":"Unveiling a longstanding misinterpretation: revisiting phylogenetic and morphological evidence from <i>Arabis verna</i> (L.) W.T.Aiton, supports the description of a monospecific taxon, <i>Pseudoarabis</i> A.R. Khosravi & A. Eslami-Farouji <i>gen. nov</i>.","authors":"Ahmad Reza Khosravi, Özlem Çetin, Atena Eslami-Farouji","doi":"10.22099/mbrc.2026.55558.2272","DOIUrl":"10.22099/mbrc.2026.55558.2272","url":null,"abstract":"<p><p>The tribe Arabideae includes various species worldwide with ornamental features; however, it has undergone taxonomic revisions and has been reclassified into different genera. Despite the available literature, the taxonomic assignment of some taxa requires further consideration. This study therefore addresses the true taxonomic position of <i>Arabis verna</i> (L.) W.T.Aiton, which is not phylogenetically nested within other <i>Arabis</i> species but is instead closely related to <i>Aubrieta</i> Adans,. The species is naturally distributed in Southwest Asia, North Africa, and South Europe, and its taxonomic delimitation has remained unresolved. Phylogenetic evidence from previous authorities, together with our morphological observations, supports the distinct status of <i>A. verna</i> from the genus <i>Aubrieta</i>. Consequently, <i>A. verna</i> is excluded from <i>Aubrieta</i> and transferred to a newly established genus, <i>Pseudoarabis</i> A.R. Khosravi & A. Eslami-Farouji gen. nov., and the new combination, <i>P. verna</i> (L.) A.R. Khosravi & A. Eslami-Farouji comb. nov. is proposed.</p>","PeriodicalId":19025,"journal":{"name":"Molecular Biology Research Communications","volume":"15 3","pages":"175-186"},"PeriodicalIF":1.4,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13370757/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148456377","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Hooman Rezaie, Sanaz Dastghaib, Morvarid Siri, Pooneh Mokarram, Mina Hemmati
{"title":"CPUK02 sensitizes U87 glioblastoma cell lines to TMZ treatment via autophagy flux inhibition.","authors":"Hooman Rezaie, Sanaz Dastghaib, Morvarid Siri, Pooneh Mokarram, Mina Hemmati","doi":"10.22099/mbrc.2025.52011.2079","DOIUrl":"10.22099/mbrc.2025.52011.2079","url":null,"abstract":"<p><p>Adjuvant chemotherapy with TMZ (Temozolomide) does not improve the survival of patients suffering from GBM (Glioblastoma). Given the importance of autophagy and UPR (Unfolding Protein Response) in chemotherapy resistance, as well as the role of <i>Beclin-1, LC3IIβ</i>, and <i>P62</i> in the regulation of autophagy, we evaluated the effect of TMZ along with CPUK02 on U87 cells as a model of Glioblastoma cancer in this study. To achieve this goal, we treated the U87 cells with different doses of TMZ (50, 100, 200, 400, and 800 μM) and CPUK02 (1, 0.5, 0.25, 0.125, 0.06, 0.03, 0.01, and 0.007 μM); then, cell viability was assessed by MTT assay. The gene expression of <i>Beclin1, P62, LC3IIβ,</i> and <i>XBP-1s</i> was analyzed using quantitative real-time polymerase chain reaction. The comparison of the control group with the groups treated with the TMZ drug showed that, in 48 and 72 hours, doses of TMZ more than IC<sub>50</sub> (100 μM) (<i>p</i><0.001) significantly led to cell death. CPUK02 doses more than 0.125 (<i>p</i><0.0001) significantly led to cell death. TMZ and CPUK02 combination therapy (100 and 0.03 μM, respectively) increased the expression of <i>Beclin-1, LC3IIβ</i>, and <i>P62</i> and activated the IRE-1 arm of UPR by increasing the expression of XBP-1s. TMZ and CPUK02 treatment inhibits the autophagic flux (<i>p62, LC3IIβ</i>). Increased <i>XBP-1s</i> expression might contribute to the enhanced TMZ sensitivity. This combination therapy is promising for TMZ-resistant cancers, but it needs further investigation.</p>","PeriodicalId":19025,"journal":{"name":"Molecular Biology Research Communications","volume":"15 1","pages":"11-20"},"PeriodicalIF":1.0,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12673630/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145678261","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Molecular and Morphological evidence support the delimitation of a new genus, <i>Hafezia gen. nov</i>. in Arabideae (Brassicaceae).","authors":"Ahmad Reza Khosravi, Atena Eslami-Farouji","doi":"10.22099/mbrc.2025.54085.2198","DOIUrl":"10.22099/mbrc.2025.54085.2198","url":null,"abstract":"<p><p>Recent molecular phylogenetic analyses within the tribe Arabideae (Brassicaceae) have uncovered unresolved lineages that challenge current generic boundaries. In this study, we incorporate molecular data with morphological evidence to resolve a long-standing taxonomic ambiguity, resulting in the description of a new monophyletic genus, <i>Hafezia</i> gen. nov., together with two new combinations, <i>H. aucheri</i> (Boiss.) A.R. Khosravi & A. Eslami-Farouji and <i>H. parvula</i> (Dufour ex DC.) A.R. Khosravi & A. Eslami-Farouji<i>.</i> Integrative taxonomy and phylogenetic insights, such as indels and substitution nucleotide variants, confirm the distinct assignment of these taxa, previously misassigned to <i>Arabis</i> L. Morphological reassessment, including traits such as simple, long setaceous hairs, notched petals, winged stamens, not compressed, not subtorulose or torulose fruits, supports their separation. The new genus naturally grows in the Mediterranean and west of the Irano-Turanian floristic regions. Our findings highlight the significance of integration of taxonomic investigations with the molecular investigations in clarifying evolutionary relationships and provide a revised key for accurate identification within Arabideae.</p>","PeriodicalId":19025,"journal":{"name":"Molecular Biology Research Communications","volume":"15 2","pages":"117-130"},"PeriodicalIF":1.4,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13148450/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147840230","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Mehdi Ghavamizadeh, Roozbeh Kiani, Fatemeh Shams, Parmis Taghizadeh, Ali Honari-Jahromi, Seyed Mohammad Hossein Afzali-Joibari, Mozhdeh Zamani, Sanaz Dastghaib, Pooneh Mokarram
{"title":"A systematic review on the potential of modulating the IRE arm of the UPR in U87 and U251 glioblastoma cells for improved therapeutic efficacy.","authors":"Mehdi Ghavamizadeh, Roozbeh Kiani, Fatemeh Shams, Parmis Taghizadeh, Ali Honari-Jahromi, Seyed Mohammad Hossein Afzali-Joibari, Mozhdeh Zamani, Sanaz Dastghaib, Pooneh Mokarram","doi":"10.22099/mbrc.2025.54152.2205","DOIUrl":"10.22099/mbrc.2025.54152.2205","url":null,"abstract":"<p><p>Glioblastoma multiforme (GBM) remains the most aggressive primary brain tumor with poor prognosis and limited response to current therapies. Recent studies suggest that the unfolded protein response (UPR), particularly the inositol-requiring enzyme 1 (IRE1) signaling arm, plays a pivotal role in GBM pathophysiology by mediating cellular adaptation to endoplasmic reticulum stress. This systematic review evaluates the role of IRE1 in GBM cell lines (U87, U251) and investigates whether its activation or inhibition affects migration, proliferation, apoptosis, and cell death. A comprehensive search was conducted on PubMed/ Medline, Scopus, Web of Science, and Embase using various keywords up to October 14, 2025, following the PRISMA guidelines. The search aimed to identify original English-language studies that specifically examined and analyzed the IRE1 arm of the UPR pathway in glioblastoma cells. Out of 466 records, 26 studies met the inclusion criteria. Twenty studies explored IRE1 activation, while six investigated its inhibition. IRE1 activation yielded dual effects-promoting apoptosis via JNK or XBP1 pathways in some contexts, while supporting tumor survival and angiogenesis through XBP1-mediated transcription and RIDD suppression in others. Dual role of IRE1 could sensitize GBM cells to chemotherapy agents, reduced migration and proliferation, and induced apoptosis. IRE1 acts as a context-dependent regulator in GBM, showing both pro-survival and pro-death roles. Most studies report that IRE1 activation promotes glioblastoma cell death, while fewer address its inhibition. Thus, both activation and inhibition may offer therapeutic potential depending on cellular context and downstream signaling.</p>","PeriodicalId":19025,"journal":{"name":"Molecular Biology Research Communications","volume":"15 2","pages":"85-101"},"PeriodicalIF":1.4,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13148453/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147840630","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"<i>Staphylococcus aureus</i> aggravates psoriasis in human keratinocytes with the assistance of IL-17A and TNF- α, along with a contribution from genes associated with skin cutaneous melanoma.","authors":"Dawood Ali-Adel, Zabn Mawj-Saddam","doi":"10.22099/mbrc.2025.54205.2207","DOIUrl":"10.22099/mbrc.2025.54205.2207","url":null,"abstract":"<p><p>Psoriasis patients were 4- 5 times more likely to have S. aureus colonize their skin. Psoriasis is caused by staphylococcal infection-induced keratinocyte death, which is maintained by elevated cytokine production of TNF-α and IFN-γ. The study sought to determine the association between the influence of gene expression of certain genes in psoriasis infections in the presence of S. aureus and their effect in Skin Cutaneous Melanoma infections. GEO with accession number (GSE207390) was used to acquire the data. The microarray test was used to perform this investigation. Six sets of keratinocytes, IL-17A, and TNF-α were cultivated together. Several kinds of bioinformatics tools were employed to fulfill the study's objective. Gene hub analysis of 34284 genes was scanned. Six genes demonstrated high expression rates were expressed during the metastatic stage: <i>CCL27</i>, <i>IL19</i>, <i>PAPPA2</i>, <i>UHRF1</i>, <i>IFNAR2</i>, and <i>GLS2</i>. <i>IFNAR2</i> and <i>UHRF1</i> had the highest levels of expression. The expression of the <i>COL4A4</i> gene rose in response to sun exposure, but the expression of the other genes remained same. The existence of cytokine groups with <i>S. aureus</i> in keratinocytes influences the expression difference compared to the other groups. This work adds to our understanding of the molecular alterations that occur in the epidermis of psoriasis patients, as well as their relationship to comorbidities.</p>","PeriodicalId":19025,"journal":{"name":"Molecular Biology Research Communications","volume":"15 3","pages":"135-143"},"PeriodicalIF":1.4,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13370756/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148456313","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Response to the Letter: Observations and points of interest regarding bioinformatics predictions of miRNA targeting syncytin genes in endometriosis and miscarriage.","authors":"Somayeh Shatizadeh-Malekshahi","doi":"10.22099/mbrc.2025.55184.2256","DOIUrl":"10.22099/mbrc.2025.55184.2256","url":null,"abstract":"","PeriodicalId":19025,"journal":{"name":"Molecular Biology Research Communications","volume":"15 2","pages":"133"},"PeriodicalIF":1.4,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13148449/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147840235","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}