Methylenetetrahydrofolate reductase C677T and A1298C polymorphisms and fluorouracil-based treatment in Taiwan colorectal cancer. Issue 8 (September 2015)
- Record Type:
- Journal Article
- Title:
- Methylenetetrahydrofolate reductase C677T and A1298C polymorphisms and fluorouracil-based treatment in Taiwan colorectal cancer. Issue 8 (September 2015)
- Main Title:
- Methylenetetrahydrofolate reductase C677T and A1298C polymorphisms and fluorouracil-based treatment in Taiwan colorectal cancer
- Authors:
- Wu, Nai-Chun
Su, Shih-Ming
Lin, Tai-Jung
Chin, Jen
Hou, Chun-Fang
Yang, Jhong-Ying
Liu, Wen-Sheng
Chang, Li-Ching - Abstract:
- <abstract> <title> <x xml:space="preserve">Abstract</x> </title> <sec> <p>This study aimed to investigate the association between methylenetetrahydrofolate reductase (<italic>MTHFR</italic>) gene polymorphisms and the prognosis of colorectal cancer (CRC) patients undergoing 5-fluorouracil (5-FU)-based chemotherapy in Taiwan. We investigated 126 CRC cases. The most common polymorphisms C677T (rs1801133) and A1298C (rs1801131) in <italic>MTHFR</italic> were genotyped using PCR-restriction fragment length polymorphism. The frequencies of C677T and A1298C were further compared with those in the HapMap database for Whites and Asians. In this study, we found that TT-homozygosity at <italic>MTHFR</italic> C677T was significantly associated with survival in CRC patients [<italic>P</italic>&lt;0.001; 95% confidence interval (CI)=0.068–0.212]. In CRC patients receiving 5-FU-based chemotherapy, the TT genotype at C677T was also significantly associated with survival (<italic>P</italic>=0.001; 95% CI=0.113–0.400) and recurrence after surgery (<italic>P</italic>&lt;0.001; 95% CI=0.295–0.609). The A1298C genotypes had a significant impact on survival (<italic>χ</italic><sup>2</sup>=7.103; <italic>P</italic>=0.029). The <italic>MTHFR</italic> A1298C CC genotype may increase the risk of death in Taiwanese CRC patients. The <italic>MTHFR</italic> C677T TT genotype was present at a lower frequency in our CRC patients than in the HapMap Asian population, but the frequency was similar to that<abstract> <title> <x xml:space="preserve">Abstract</x> </title> <sec> <p>This study aimed to investigate the association between methylenetetrahydrofolate reductase (<italic>MTHFR</italic>) gene polymorphisms and the prognosis of colorectal cancer (CRC) patients undergoing 5-fluorouracil (5-FU)-based chemotherapy in Taiwan. We investigated 126 CRC cases. The most common polymorphisms C677T (rs1801133) and A1298C (rs1801131) in <italic>MTHFR</italic> were genotyped using PCR-restriction fragment length polymorphism. The frequencies of C677T and A1298C were further compared with those in the HapMap database for Whites and Asians. In this study, we found that TT-homozygosity at <italic>MTHFR</italic> C677T was significantly associated with survival in CRC patients [<italic>P</italic>&lt;0.001; 95% confidence interval (CI)=0.068–0.212]. In CRC patients receiving 5-FU-based chemotherapy, the TT genotype at C677T was also significantly associated with survival (<italic>P</italic>=0.001; 95% CI=0.113–0.400) and recurrence after surgery (<italic>P</italic>&lt;0.001; 95% CI=0.295–0.609). The A1298C genotypes had a significant impact on survival (<italic>χ</italic><sup>2</sup>=7.103; <italic>P</italic>=0.029). The <italic>MTHFR</italic> A1298C CC genotype may increase the risk of death in Taiwanese CRC patients. The <italic>MTHFR</italic> C677T TT genotype was present at a lower frequency in our CRC patients than in the HapMap Asian population, but the frequency was similar to that in Whites in the HapMap database. The distribution of <italic>MTHFR</italic> A1298C genotypes was similar in our CRC and in the HapMap Asian population, but was different from that in the White population. This study suggested that <italic>MTHFR</italic> C677T and A1298C are associated with prognosis in CRC patients undergoing 5-FU-based chemotherapy.</p> </sec> </abstract> … (more)
- Is Part Of:
- Anti-cancer drugs. Volume 26:Issue 8(2015)
- Journal:
- Anti-cancer drugs
- Issue:
- Volume 26:Issue 8(2015)
- Issue Display:
- Volume 26, Issue 8 (2015)
- Year:
- 2015
- Volume:
- 26
- Issue:
- 8
- Issue Sort Value:
- 2015-0026-0008-0000
- Page Start:
- Page End:
- Publication Date:
- 2015-09
- Subjects:
- Antineoplastic agents -- Periodicals
Cancer -- Chemotherapy -- Periodicals
Antineoplastic Agents -- therapeutic use -- Periodicals
Drug Therapy -- Periodicals
616.994061 - Journal URLs:
- http://ovidsp.ovid.com/ovidweb.cgi?T=JS&NEWS=n&CSC=Y&PAGE=toc&D=yrovft&AN=00001813-000000000-00000 ↗
http://ovidsp.tx.ovid.com/spb/ovidweb.cgi ↗
http://www.anti-cancerdrugs.com/ ↗
http://journals.lww.com/pages/default.aspx ↗
http://firstsearch.oclc.org ↗ - DOI:
- 10.1097/CAD.0000000000000261 ↗
- Languages:
- English
- ISSNs:
- 0959-4973
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 1547.287300
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