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DOI 10.19746/j.cnki.issn.1009-2137.2025.01.018

Медицинская библиотека · Zhongguo shi yan xue ye xue za zhi · 2025

[Screening and Preliminary Validation of Multiple Myeloma Specific Proteins].

Zhao Shan, Liu Hui-Hui, Yang Xiao-Ying, Xie Wei-Wei, Xue Chao, He Xiao-Ya, Wang Jin, Dong Yu-Jun

Аннотация на английскомСтатьяПеревод пока не подготовлен

Аннотация

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.

Для цитирования: Zhao Shan, Liu Hui-Hui, Yang Xiao-Ying, Xie Wei-Wei, Xue Chao, He Xiao-Ya, Wang Jin, Dong Yu-Jun. [Screening and Preliminary Validation of Multiple Myeloma Specific Proteins].. Zhongguo shi yan xue ye xue za zhi. 2025. DOI: 10.19746/j.cnki.issn.1009-2137.2025.01.018.

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