Evidence map›Paper›PMID 39607580›Full record

ArticleClinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico2025

Association of hTERT MNS16A polymorphism with clinical outcomes of North Indian lung cancer patients undergoing platinum-based doublet chemotherapy.

Ishmeet Kaur, Heena Kansal, Sidhartha Singh, Navneet Singh, Siddharth Sharma

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Article in Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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5 authors.

Ishmeet KaurDepartment of Biotechnology, Thapar Institute of Engineering and Technology, Patiala, Punjab, 147004, India.
Heena KansalDepartment of Biotechnology, Thapar Institute of Engineering and Technology, Patiala, Punjab, 147004, India.
Sidhartha SinghDepartment of Biosciences and Bioengineering, D Y Patil International University, Akurdi, Pune, Maharashtra, India.
Navneet SinghDepartment of Pulmonary Medicine, Post Graduate Institute of Medical Education and Research (PGIMER), Chandigarh, India.
Siddharth SharmaDepartment of Biotechnology, Thapar Institute of Engineering and Technology, Patiala, Punjab, 147004, India. siddharthsharma.phd@thapar.edu.ORCID http://orcid.org/0000-0001-9414-3771

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6 · The paper itself

Abstract

backgroundTelomerase has been linked to aging and cancer. The MNS16A polymorphism in the hTERT gene plays a significant role in modulating telomerase activity and highlights the complexity of telomere-related genetics in cancer research. EXPERIMENTAL

designWe genotyped 401 lung-cancer samples treated with platinum-based chemotherapy to identify the MNS16A polymorphism. We assessed overall survival using the Kaplan-Meier method and Cox regression analysis for adjusted hazard ratios. Stratified analyses evaluated risks for subgroups based on clinicopathologic parameters, outcomes, and toxicity calculated.

resultsOur findings show no significant link between MNS16A polymorphism and lung-cancer survival. However, in squamous cell carcinoma (SQCC) patients, the SS genotype was associated with poorer survival (p = 0.004). Patients with LS + SS genotypes responded better to gemcitabine in univariate (p = 0.003) and multivariate analyses (p = 0.014). The LS genotype was linked to a lower risk of progression to stage 4 (p = 0.011) and metastasis (p = 0.015) but an increased risk of T4 tumor size (p = 0.026). No significant correlations were found between MNS16A polymorphism and treatment-related toxicities.

conclusionThe MNS16A polymorphism does not significantly impact overall lung-cancer survival but affects specific subgroups, influencing certain lung-cancer subtypes and treatment responses while having limited predictive value for overall outcomes or toxicity risks.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsCarcinoma, Non-Small-Cell LungCarcinoma, Squamous CellLung NeoplasmsPolymorphism, GeneticTelomeraseAdultAgedCarboplatinCisplatinDeoxycytidineFemaleGemcitabineGenotypeHumansIndiaCarboplatinCisplatinDeoxycytidineGemcitabineTelomeraseTERT protein, humanLung CancerMNS16APolymorphismTelomerase

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.