Screening and Preliminary Validation of Multiple Myeloma Specific Proteins.
10.19746/j.cnki.issn.1009-2137.2025.01.018
- Author:
Shan ZHAO
1
;
Hui-Hui LIU
1
;
Xiao-Ying YANG
1
;
Wei-Wei XIE
1
;
Chao XUE
1
;
Xiao-Ya HE
1
;
Jin WANG
1
;
Yu-Jun DONG
1
Author Information
1. Department of Hematology, Peking University First Hospital, Beijing 100032, China.
- Publication Type:Journal Article
- Keywords:
multiple myeloma;
targeted protein;
bioinformatics
- MeSH:
Humans;
Multiple Myeloma/genetics*;
Cell Line, Tumor;
Proteins/metabolism*;
Computational Biology;
RNA, Messenger/genetics*
- From:
Journal of Experimental Hematology
2025;33(1):127-132
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To screen novel diagnostic marker or therapeutic target for multiple myeloma (MM).
METHODS:Sel1L, SPAG4, KCNN3 and PARM1 were identified by bioinformatics method based on GEO database as high expression genes in MM. Their RNA and protein expression levels in bone marrow mononuclear cells from myeloma cell lines U266, NCI-H929, MM.1s, RPMI8226 and leukemia cell line THP1, as well as 31 MM patients were evaluated by RT-PCR and Western blot, respectively. Meanwhile, 5 samples of bone marrow from healthy donors for allogeneic hematopoietic stem cell transplantation were employed as controls.
RESULTS:Compared with leukemia cell line THP1, the expression levels of KCNN3, PARM1 and Sel1L mRNA were significantly increased in myeloma cell lines U266, NCI-H929 and MM.1s, while PARM1 was further increased in myeloma cell lines 8226. Western blot showed that the 4 genes were all expressed in the 4 myeloma cell lines. Compared with healthy controls, the expression levels of Sel1L, SPAG4, KCNN3 and PARM1 mRNA were significantly higher in MM patients (all P < 0.05). Western blot showed that the 4 genes were all expressed in MM patients, and the protein expression level of Sel1L and KCNN3 were significantly different compared with healthy donors (all P < 0.01).
CONCLUSION:Sel1L, SPAG4, KCNN3 and PARM1 may be potential diagnostic markers and therapeutic targets for MM.
