Latent infection of human cytomegalovirus is associated with the development of gastric cancer
Author(s) -
Jinji Jin,
Changyuan Hu,
Pengfei Wang,
Jing Chen,
Tiantian Wu,
Wenjing Chen,
Lulu Ye,
Guangbao Zhu,
Lifang Zhang,
Xiangyang Xue,
Xian Shen
Publication year - 2014
Publication title -
oncology letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.766
H-Index - 54
eISSN - 1792-1082
pISSN - 1792-1074
DOI - 10.3892/ol.2014.2148
Subject(s) - human cytomegalovirus , oncogene , cancer , locus (genetics) , biology , gene , molecular medicine , polymerase chain reaction , viral oncogene , cell cycle , immunology , virus , virology , genetics
The worldwide contagion, human cytomegalovirus (HCMV), may cause a series of disorders in infected individuals. The aim of the present study was to investigate whether HCMV infection is associated with the development of gastric cancer. In this study, the positive expression of unique long (UL)133-UL138 and immediate-early (IE)1 genes, which are associated with viral latency and replication, respectively, were detected using nested polymerase chain reaction. A χ 2 test and logistic regression analysis were performed to further investigate the preliminary data. The data indicated that the positive rate of UL133, UL135 and UL136 expression in cancer tissues was higher than that in paired normal tissues (P=0.01, 0.027 and 0.013, respectively). However, no significant differences were identified in the UL133-138 locus and IE1 gene when associated with clinicopathological features. Furthermore, seven infection patterns were identified, with the UL133 + UL138 infection pattern representing the largest proportion in the cancer (60.34%) and normal tissues (42.11%). In conclusion, it is possible that the UL133-UL138 locus is important in the occurrence of gastric cancer. The mechanism by which UL133-UL138 locus expression differs in human gastric cancer requires further investigation.
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