TY - JOUR
T1 - CCNJ detected by triple combination array analysis as a tumor-related gene of hepatocellular carcinoma
AU - Takano, Nao
AU - Hishida, Mitsuhiro
AU - Inokawa, Yoshikuni
AU - Hayashi, Masamichi
AU - Kanda, Mitsuro
AU - Nishikawa, Yoko
AU - Iwata, Naoki
AU - Kobayashi, Daisuke
AU - Tanaka, Chie
AU - Yamada, Suguru
AU - Nakayama, Goro
AU - Fujii, Tsutomu
AU - Sugimoto, Hiroyuki
AU - Koike, Masahiko
AU - Fujiwara, Michitaka
AU - Kodera, Yasuhiro
AU - Nomoto, Shuji
N1 - Publisher Copyright:
© 2015, Spandidos Publications. All rights reserved.
PY - 2015/5/1
Y1 - 2015/5/1
N2 - Hepatocellular carcinoma (HCC) has a high likelihood of recurrence and a poor prognosis. To detect cancer-related genes of HCC, we developed a new technique: triple combination array analysis, consisting of a methylation array, a gene expression array and a single nucleotide polymorphism array. A surgical specimen obtained from a 68-year-old female HCC patient was analyzed using triple combination array, which identified cyclin J (CCNJ) as a candidate cancer-related gene of HCC. Subsequently, samples from 85 HCC patients were evaluated for CCNJ promoter hypermethylation and expression status using methylation-specific PCR (MSP) and quantitative reverse transcriptase RT-PCR, respectively. CCNJ was found to be hypermethylated (methylation value, 0.906; range, 0-1.0) in cancer tissue, compared with adjacent non-cancerous tissue (0.112) using a methylation array. MSP revealed that CCNJ was hypermethylated in 67 (78.8%) of the tumor samples. CCNJ expression was significantly decreased in cases with hypermethylation (P<0.0001). Furthermore, cases with both promoter hypermethylation and decreased expression of CCNJ in the tumor tissue had a worse overall survival than the other cases (P=0.0383). In conclusion, our results indicated that CCNJ could be a novel prognostic marker of HCC, and this study indicated that triple combination array analysis was effective in detecting new tumor-related genes and their mechanisms.
AB - Hepatocellular carcinoma (HCC) has a high likelihood of recurrence and a poor prognosis. To detect cancer-related genes of HCC, we developed a new technique: triple combination array analysis, consisting of a methylation array, a gene expression array and a single nucleotide polymorphism array. A surgical specimen obtained from a 68-year-old female HCC patient was analyzed using triple combination array, which identified cyclin J (CCNJ) as a candidate cancer-related gene of HCC. Subsequently, samples from 85 HCC patients were evaluated for CCNJ promoter hypermethylation and expression status using methylation-specific PCR (MSP) and quantitative reverse transcriptase RT-PCR, respectively. CCNJ was found to be hypermethylated (methylation value, 0.906; range, 0-1.0) in cancer tissue, compared with adjacent non-cancerous tissue (0.112) using a methylation array. MSP revealed that CCNJ was hypermethylated in 67 (78.8%) of the tumor samples. CCNJ expression was significantly decreased in cases with hypermethylation (P<0.0001). Furthermore, cases with both promoter hypermethylation and decreased expression of CCNJ in the tumor tissue had a worse overall survival than the other cases (P=0.0383). In conclusion, our results indicated that CCNJ could be a novel prognostic marker of HCC, and this study indicated that triple combination array analysis was effective in detecting new tumor-related genes and their mechanisms.
KW - Cancer-related gene
KW - Cyclin J
KW - Hepatocellular carcinoma
KW - Methylation
KW - Triple combination array
UR - http://www.scopus.com/inward/record.url?scp=84925434514&partnerID=8YFLogxK
U2 - 10.3892/ijo.2015.2892
DO - 10.3892/ijo.2015.2892
M3 - 学術論文
C2 - 25672416
AN - SCOPUS:84925434514
SN - 1019-6439
VL - 46
SP - 1963
EP - 1970
JO - International Journal of Oncology
JF - International Journal of Oncology
IS - 5
ER -