Indian journal of pathology & microbiology · 2026
Protective role of TGF-β1 (-509C>T, rs1800469) single-nucleotide polymorphism against radiation toxicities in locally advanced head and neck cancer.
СтатьяНаблюдательное исследованиеНазвание и аннотация: Перевод пока не подготовлен
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Krishnan M P Sarath, Goyal Bela, Gupta Sweety, Christudass Christhunesa S, Solomon Raja, Mirza Anissa A, Gupta Amit, Chaudhary Nitin, Prajapati Ayush, Mistry Satarupa
Аннотация
BACKGROUND: Head and neck cancer (HNC), predominantly head and neck squamous cell carcinoma (HNSCC), poses a significant health burden globally. Intensity-modulated radiation therapy (IMRT) has improved outcomes in HNC; however, radiation-induced toxicities, particularly oral mucositis and dermatitis, remain critical concerns. Genetic variations, such as single-nucleotide polymorphisms (SNPs) in the TGF-β1 gene (-509C>T, rs1800469), may modulate these toxicities and impact treatment response.
MATERIALS AND METHODS: This observational analytical study included 50 patients with locally advanced HNC undergoing IMRT at a tertiary care center in North India. Genotyping of TGF-β1 (-509C>T, rs1800469) was conducted using PCR-RFLP. Acute radiation toxicities were assessed weekly during IMRT and graded using CTCAE v4.0. Radiotherapy response was evaluated three months posttreatment using RECIST v1.1. Statistical analyses, including Chi-square test, multivariate regression, explored associations between genotypes, toxicities, and treatment outcomes.
RESULTS: The cohort comprised 50 patients (94% male, mean age: 53.3 ± 12.35 years). TGF-β1 (-509C>T, rs1800469) genotypes were distributed as CC (48%), TC (30%), and TT (22%), conforming to the Hardy-Weinberg equilibrium. Grade 1 oral mucositis and dermatitis occurred in 48% and 56%, respectively, with higher grades in 52% and 44%. The CC genotype was significantly associated with reduced risk of severe oral mucositis (P = 0.046; OR = 0.31), while the TC genotype conferred protection against severe dermatitis (P = 0.035; OR = 0.26).
CONCLUSION: The CC and TC genotypes of TGF-β1 (-509C>T, rs1800469) exhibit protective roles against acute radiation toxicities in HNC patients receiving IMRT. These findings underscore the potential of TGF-β1 SNPs as biomarkers for toxicity risk stratification, enabling personalized therapeutic approaches.
MATERIALS AND METHODS: This observational analytical study included 50 patients with locally advanced HNC undergoing IMRT at a tertiary care center in North India. Genotyping of TGF-β1 (-509C>T, rs1800469) was conducted using PCR-RFLP. Acute radiation toxicities were assessed weekly during IMRT and graded using CTCAE v4.0. Radiotherapy response was evaluated three months posttreatment using RECIST v1.1. Statistical analyses, including Chi-square test, multivariate regression, explored associations between genotypes, toxicities, and treatment outcomes.
RESULTS: The cohort comprised 50 patients (94% male, mean age: 53.3 ± 12.35 years). TGF-β1 (-509C>T, rs1800469) genotypes were distributed as CC (48%), TC (30%), and TT (22%), conforming to the Hardy-Weinberg equilibrium. Grade 1 oral mucositis and dermatitis occurred in 48% and 56%, respectively, with higher grades in 52% and 44%. The CC genotype was significantly associated with reduced risk of severe oral mucositis (P = 0.046; OR = 0.31), while the TC genotype conferred protection against severe dermatitis (P = 0.035; OR = 0.26).
CONCLUSION: The CC and TC genotypes of TGF-β1 (-509C>T, rs1800469) exhibit protective roles against acute radiation toxicities in HNC patients receiving IMRT. These findings underscore the potential of TGF-β1 SNPs as biomarkers for toxicity risk stratification, enabling personalized therapeutic approaches.