Impact of epidermal growth factor single‐nucleotide polymorphism on recurrence of hepatocellular carcinoma after hepatectomy in patients with chronic hepatitis C virus infection. Issue 6 (15th May 2014)
- Record Type:
- Journal Article
- Title:
- Impact of epidermal growth factor single‐nucleotide polymorphism on recurrence of hepatocellular carcinoma after hepatectomy in patients with chronic hepatitis C virus infection. Issue 6 (15th May 2014)
- Main Title:
- Impact of epidermal growth factor single‐nucleotide polymorphism on recurrence of hepatocellular carcinoma after hepatectomy in patients with chronic hepatitis C virus infection
- Authors:
- Yoshiya, Shohei
Fujimoto, Yukiko
Bekki, Yuki
Konishi, Hideyuki
Yamashita, Yo‐ichi
Ikegami, Toru
Yoshizumi, Tomoharu
Shirabe, Ken
Oda, Yoshinao
Maehara, Yoshihiko - Abstract:
- <abstract abstract-type="main" id="cas12415-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Epidermal growth factor (EGF) gene single‐nucleotide polymorphism (SNP) is associated with an increased risk of hepatic tumors. The study aimed to elucidate the impact of EGF SNP and EGF receptor (EGFR) expression on the recurrence of hepatocellular carcinoma (HCC) after hepatectomy. To examine the impact of EGF SNP and EGFR on recurrent HCC, we retrospectively analyzed 141 HCC patients with chronic hepatitis C virus infection who underwent curative hepatectomy. The EGF *61 GG allele was present in 69 patients (48.9%), AG in 56 (39.7%) and AA in 16 (11.4%). The AA group had a significantly lower rate of intrahepatic metastasis (0% <italic>vs</italic> 16.5%, <italic>P = </italic>0.02), lower serum EGF concentration (26.3 ± 15.9 pg/mL <italic>vs</italic> 43.4 ± 30.5 pg/mL, <italic>P = </italic>0.02) and lower proportion of early recurrence (≤2 years; 28.6% <italic>vs</italic> 71.2%, <italic>P = </italic>0.03) than the AG/GG group. The AA group had significantly higher recurrence‐free survival than the AG/GG group (<italic>P = </italic>0.04), but there was no significant difference in overall survival between these two groups (<italic>P = </italic>0.97). High versus low EGFR expression analyzed by immunohistochemical staining in cancer cells was not significantly associated with overall survival (<italic>P = </italic>0.37) or recurrence‐free survival<abstract abstract-type="main" id="cas12415-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Epidermal growth factor (EGF) gene single‐nucleotide polymorphism (SNP) is associated with an increased risk of hepatic tumors. The study aimed to elucidate the impact of EGF SNP and EGF receptor (EGFR) expression on the recurrence of hepatocellular carcinoma (HCC) after hepatectomy. To examine the impact of EGF SNP and EGFR on recurrent HCC, we retrospectively analyzed 141 HCC patients with chronic hepatitis C virus infection who underwent curative hepatectomy. The EGF *61 GG allele was present in 69 patients (48.9%), AG in 56 (39.7%) and AA in 16 (11.4%). The AA group had a significantly lower rate of intrahepatic metastasis (0% <italic>vs</italic> 16.5%, <italic>P = </italic>0.02), lower serum EGF concentration (26.3 ± 15.9 pg/mL <italic>vs</italic> 43.4 ± 30.5 pg/mL, <italic>P = </italic>0.02) and lower proportion of early recurrence (≤2 years; 28.6% <italic>vs</italic> 71.2%, <italic>P = </italic>0.03) than the AG/GG group. The AA group had significantly higher recurrence‐free survival than the AG/GG group (<italic>P = </italic>0.04), but there was no significant difference in overall survival between these two groups (<italic>P = </italic>0.97). High versus low EGFR expression analyzed by immunohistochemical staining in cancer cells was not significantly associated with overall survival (<italic>P = </italic>0.37) or recurrence‐free survival (<italic>P = </italic>0.39). Therefore, EGF *61 AA was associated with a lower risk of recurrence after curative hepatectomy for HCC in patients with hepatitis C virus infection than other genotypes, but EGFR expression in cancer cells was not significantly associated with prognosis.</p> </abstract> … (more)
- Is Part Of:
- Cancer science. Volume 105:Issue 6(2014:Jun.)
- Journal:
- Cancer science
- Issue:
- Volume 105:Issue 6(2014:Jun.)
- Issue Display:
- Volume 105, Issue 6 (2014)
- Year:
- 2014
- Volume:
- 105
- Issue:
- 6
- Issue Sort Value:
- 2014-0105-0006-0000
- Page Start:
- 646
- Page End:
- 650
- Publication Date:
- 2014-05-15
- Subjects:
- Cancer -- Periodicals
Neoplasms -- Periodicals
Research -- Periodicals
Electronic journals
616.994005 - Journal URLs:
- http://firstsearch.oclc.org ↗
http://firstsearch.oclc.org/journal=1347-9032;screen=info;ECOIP ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1349-7006 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/cas.12415 ↗
- Languages:
- English
- ISSNs:
- 1347-9032
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3046.603000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 4036.xml