Evidence map›Paper›PMID 23136537›Full record

ArticleInternational journal of medical sciences2012

THRB genetic polymorphisms can predict severe myelotoxicity after definitive chemoradiotherapy in patients with esophageal squamous cell carcinoma.

Ikuya Miki, Tsutomu Nakamura, Akiko Kuwahara, Motohiro Yamamori, Kohshi Nishiguchi, Takao Tamura, Tatsuya Okuno, Hideaki Omatsu, Shigeto Mizuno, Midori Hirai and 2 more

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Article in International journal of medical sciences, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 33% of its field
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 2 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

12 authors at 6 institutions in 1 country.

Ikuya MikiDepartment of Gastroenterology, Kobe University Graduate School of Medicine, Kobe, Japan.
Tsutomu Nakamura
Akiko Kuwahara
Motohiro Yamamori
Kohshi Nishiguchi
Takao Tamura
Tatsuya Okuno
Hideaki Omatsu
Shigeto Mizuno
Midori Hirai
Takeshi Azuma
Toshiyuki Sakaeda
Kobe University · JPKobe University Hospital · JPHimeji Dokkyo University · JPKobe Pharmaceutical University · JPKyoto University · JPMukogawa Women's University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveChemotherapy-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).

methodsForty-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.

resultsDistribution 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%).

conclusionsTHRB intronic SNPs can provide useful information on CRT-related severe myelotoxicity in patients with ESCC. Future studies will be needed to confirm these findings.

Indexed as

Polymorphism, Single Nucleotide3' Untranslated RegionsAgedAntineoplastic Combined Chemotherapy ProtocolsAsian PeopleCarcinoma, Squamous CellCheilitisChemoradiotherapyCisplatinEsophageal NeoplasmsEsophageal Squamous Cell CarcinomaFemaleFluorouracilGene FrequencyHaplotypesHumans3' Untranslated RegionsCisplatinFluorouracilThyroid Hormone Receptors betachemoradiotherapyesophageal squamous cell carcinomaprognosis.severe acute toxicitythyroid hormone receptor beta

Identifiers

PMID23136537
PMCPMC3491433
OpenAlexW2092539440

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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.