THRB genetic polymorphisms can predict severe myelotoxicity after definitive chemoradiotherapy in patients with esophageal squamous cell carcinoma.
THRB genetic polymorphisms can predict severe myelotoxicity after definitive chemoradiotherapy in patients with esophageal squamous cell carcinoma.
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DOI:
10.7150/ijms.5081
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发表时间:
2012
影响因子:
3.6
通讯作者:
Sakaeda T
中科院分区:
文献类型:
--
作者:
Miki I;Nakamura T;Kuwahara A;Yamamori M;Nishiguchi K;Tamura T;Okuno T;Omatsu H;Mizuno S;Hirai M;Azuma T;Sakaeda T
Objective: Chemotherapy-related toxicities are difficult to predict before treatment. In this study, we investigated whether thyroid hormone receptor beta (THRB) genetic polymorphisms can serve as a potential biomarker in patients with esophageal squamous cell carcinoma (ESCC). Methods: Forty-nine Japanese patients with ESCC who received a definitive chemoradiotherapy (CRT) with 5-fluorouracil and cisplatin in conjunction with concurrent irradiation were retrospectively analyzed. Severe acute toxicities, including leukopenia, stomatitis, and cheilitis, were evaluated according to 6 single nucleotide polymorphisms (SNPs) in the gene; the intronic SNPs of rs7635707 G/T, rs6787255 A/C, rs9812034 G/T, and rs9310738 C/T and the SNPs in the 3′-untranslated region (3′-UTR) of rs844107 C/T and rs1349265 G/A. Results: Distribution of the 4 intronic SNPs, but not the 2 SNPs in the 3′-UTR, showed a significant difference between patients with and without severe acute leukopenia. Stomatitis and cheilitis were not associated with any of the 6 analyzed SNPs. Frequency of haplotype of the 4 intronic SNPs reached approximately 97% with the 2 major haplotypes G-A-G-C (73.4%) and T-C-T-T (23.5%). Conclusions: THRB intronic SNPs can provide useful information on CRT-related severe myelotoxicity in patients with ESCC. Future studies will be needed to confirm these findings.
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DOI:
10.1677/joe-08-0539
发表时间:
2009-11
期刊:
The Journal of endocrinology
影响因子:
--
作者:
Amorim BS;Ueta CB;Freitas BC;Nassif RJ;Gouveia CH;Christoffolete MA;Moriscot AS;Lancelloti CL;Llimona F;Barbeiro HV;de Souza HP;Catanozi S;Passarelli M;Aoki MS;Bianco AC;Ribeiro MO
通讯作者:
Ribeiro MO
影响因子:
3.7
作者:
López-Fontal R;Zeini M;Través PG;Gómez-Ferrería M;Aranda A;Sáez GT;Cerdá C;Martín-Sanz P;Hortelano S;Boscá L
通讯作者:
Boscá L
影响因子:
5.8
作者:
Kawa, Milosz Piotr;Grymula, Katarzyna;Machalinski, Boguslaw
通讯作者:
Machalinski, Boguslaw
影响因子:
8.5
作者:
Grymula, K.;Paczkowska, E.;Machalinski, B.
通讯作者:
Machalinski, B.
影响因子:
8.8
作者:
Kaneko K;Ito H;Konishi K;Kurahashi T;Ito T;Katagiri A;Yamamoto T;Kitahara T;Mizutani Y;Ohtsu A;Mitamura K
通讯作者:
Mitamura K