TNF rs1799964 as a Predictive Factor of Acute Toxicities in Chinese Rectal Cancer Patients Treated With Chemoradiotherapy.
dc.contributor.author | Zhang, Hui | |
dc.contributor.author | Wang, Mengyun | |
dc.contributor.author | Shi, Tingyan | |
dc.contributor.author | Shen, Lijun | |
dc.contributor.author | Liang, Liping | |
dc.contributor.author | Deng, Yun | |
dc.contributor.author | Li, Guichao | |
dc.contributor.author | Zhu, Ji | |
dc.contributor.author | Wu, Yongxin | |
dc.contributor.author | Fan, Ming | |
dc.contributor.author | Deng, Weijuan | |
dc.contributor.author | Wei, Qingyi | |
dc.contributor.author | Zhang, Zhen | |
dc.date.accessioned | 2019-02-01T15:24:04Z | |
dc.date.available | 2019-02-01T15:24:04Z | |
dc.date.issued | 2015-11 | |
dc.date.updated | 2019-02-01T15:24:00Z | |
dc.description.abstract | Acute toxicity is the main dose-limiting factor in the chemoradiotherapy of rectal cancer patients and depends on several pro-inflammatory factors, including interleukin-1 (IL-1), IL-6, and tumor necrosis factor-alpha (TNF-α). It is unknown whether genetic factors, such as single-nucleotide polymorphisms (SNPs) in the IL-1, IL-6, and TNF genes, are also associated with acute toxicity in the process.We genotyped 5 potentially functional SNPs in these 3 genes (TNF rs1799964, TNF rs1800629, IL-6 rs1800796, and IL-1 rs1143623, IL-1 rs1143627) and estimated their associations with severe acute radiation injury (grade ≥2) in 356 rectal cancer patients.We found a predictive role of the TNF rs1799964 T variant allele in the development of acute injury (for CT vs CC: adjusted odds ratio [OR] = 4.718, 95% confidence interval [CI] = 1.152-19.328, P = 0.031; for TT vs CC: adjusted OR = 4.443, 95% CI = 1.123-17.581, P = 0.034). In the dominant model, for CT/TT vs CC, the adjusted OR = 4.132, 95% CI = 1.069-15.966, and P = 0.04.Our results suggested that genetic variants in the TNF gene may influence acute injury in rectal cancer patients treated with chemoradiotherapy and may be a predictor for personalized treatment. Additional larger and independent studies are needed to confirm our findings. | |
dc.identifier | 00005792-201511110-00024 | |
dc.identifier.issn | 0025-7974 | |
dc.identifier.issn | 1536-5964 | |
dc.identifier.uri | ||
dc.language | eng | |
dc.publisher | Ovid Technologies (Wolters Kluwer Health) | |
dc.relation.ispartof | Medicine | |
dc.relation.isversionof | 10.1097/MD.0000000000001955 | |
dc.subject | Cell Line, Tumor | |
dc.subject | Humans | |
dc.subject | Adenocarcinoma | |
dc.subject | Rectal Neoplasms | |
dc.subject | Tumor Necrosis Factor-alpha | |
dc.subject | Interleukin-1 | |
dc.subject | Interleukin-6 | |
dc.subject | Genotype | |
dc.subject | Adolescent | |
dc.subject | Adult | |
dc.subject | Aged | |
dc.subject | Aged, 80 and over | |
dc.subject | Middle Aged | |
dc.subject | Female | |
dc.subject | Male | |
dc.subject | Young Adult | |
dc.subject | Chemoradiotherapy | |
dc.title | TNF rs1799964 as a Predictive Factor of Acute Toxicities in Chinese Rectal Cancer Patients Treated With Chemoradiotherapy. | |
dc.type | Journal article | |
duke.contributor.orcid | Wei, Qingyi|0000-0002-3845-9445 | |
pubs.begin-page | e1955 | |
pubs.issue | 45 | |
pubs.organisational-group | School of Medicine | |
pubs.organisational-group | Duke | |
pubs.organisational-group | Duke Cancer Institute | |
pubs.organisational-group | Institutes and Centers | |
pubs.organisational-group | Population Health Sciences | |
pubs.organisational-group | Basic Science Departments | |
pubs.organisational-group | Medicine, Medical Oncology | |
pubs.organisational-group | Medicine | |
pubs.organisational-group | Clinical Science Departments | |
pubs.publication-status | Published | |
pubs.volume | 94 |
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