Response gene to complement 32 promotes tumorigenesis by mediating DNA damage repair and inhibits CD8+ T cells infiltration in diffuse large B-cell lymphoma

This study highlights that RGC32 is a novel molecule in DLBCL progression and might be a potential therapeutic target for DLBCL therapy.

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Publication Details

Journal
Frontiers in Immunology
Published
2025-07-16
DOI
https://doi.org/10.3389/fimmu.2025.1591615
Citations
2
Primary Topic
Complement system in diseases
Type
article
Field-Weighted Citation Impact
1.59

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article

Response gene to complement 32 promotes tumorigenesis by mediating DNA damage repair and inhibits CD8+ T cells infiltration in diffuse large B-cell lymphoma

Chunlei Shi, Xin Wang, Ling Wang, Xiyuan Zhang et al.
2 citations
Frontiers in Immunology
Complement system in diseases
1.59
article

Response gene to complement 32 promotes tumorigenesis by mediating DNA damage repair and inhibits CD8+ T cells infiltration in diffuse large B-cell lymphoma

Chunlei Shi, Xin Wang, Ling Wang, Xiyuan Zhang, Mengfei Ding, Xinting Hu, Tiange Lu
article en
2 citations

Abstract

This study highlights that RGC32 is a novel molecule in DLBCL progression and might be a potential therapeutic target for DLBCL therapy.

Frontiers in ImmunologyVol. 16
Qingdao University (CN), Shandong Provincial Hospital (CN), Affiliated Hospital of Qingdao University (CN), Shandong First Medical University (CN)
Shandong First Medical University, Key Technology Research and Development Program of Shandong
Good health and well-being
Openalex Percentile: Top 16%
Complement system in diseases
1.59
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