Expression of cancer-testis antigen in multiple myeloma.
10.1007/s11596-014-1255-7
- Author:
Li HE
1
;
Jing-na JI
;
Shang-qin LIU
;
Er XUE
;
Qing LIANG
;
Zi MA
Author Information
1. Department of Hematology, Zhongnan Hospital of Wuhan University, Wuhan, 430071, China, lihe126@hotmail.com.
- Publication Type:Journal Article
- MeSH:
Adult;
Aged;
Antigens, Neoplasm;
biosynthesis;
Cell Line, Tumor;
Gene Expression Regulation, Neoplastic;
Humans;
Male;
Middle Aged;
Multiple Myeloma;
genetics;
pathology;
Neoplasm Proteins;
biosynthesis;
Neoplasm Staging;
Repressor Proteins;
biosynthesis;
Reverse Transcriptase Polymerase Chain Reaction
- From:
Journal of Huazhong University of Science and Technology (Medical Sciences)
2014;34(2):181-185
- CountryChina
- Language:English
-
Abstract:
Recently, the immunotherapy has been highlighted among cancer treatments. Cancer-testis antigen (CTA) has been studied in a variety of solid tumors because of its specific expression in tumors, and testis, ovary and placenta tissues, but not in other normal tissues. In order to provide a new approach for multiple myeloma (MM) immunotherapy, we examined the CTA expression in MM cell lines, and primary myeloma cells in patients with MM. Reverse transcriptase-polymerase chain reaction (RT-PCR) was used to detect the mRNA expression of MAGE-C1/CT7, SSX1, SSX2 and SSX4 in MM cell lines of RPMI-8226 and U266, and bone marrow (BM) cells of 25 MM patients and 18 healthy volunteers. The results showed that the 4 CTAs were expressed in RPMI-8226 and U266 cell lines. The positive expression rate of MAGE-C1/CT7, SSX1, SSX2 and SSX4 in the BM cells of 25 MM patients was 28% (7/25), 80% (20/25), 40% (10/25) and 68% (17/25), respectively. In contrast, the expression of any member of the CTAs was not detected in BM cells of 18 healthy volunteers. The expression of two or more CTAs was detected in 80% (20/25) MM patients, and that of at least one CTA in 88% (22/25). The mRNA expression levels of SSX1 and SSX4 were significantly higher in patients with MM at stage III than in those at stage I and II (P<0.05). No statistically significant differences were observed in the mRNA expression levels of MAGE-C1/CT7 and SSX2 in further stratified analyses by age, gender, MM types and percentage of MM cells in BM (P>0.05). In conclusion, our present study showed that MAGE-C1/CT7, SSX1, SSX2 and SSX4 were co-expressed in MM cell lines and the primary myeloma cells in MM patients, but not expressed in BM cells of healthy subjects. The mRNA levels of SSX1 and SSX4 are associated with MM clinical stage. This work may provide a new insight into MM immunotherapy in the future.
