Evidence map›Paper›PMID 41439242›Full record

ArticleBlood and lymphatic cancer : targets and therapy2025

Expression and Clinical Significance of BCL2 Interacting Protein 3 Like (BNIP3L) in Serum of Patients with MM.

Yanyu Nong, Zengyi Xiong, Qicai Wang, Mengyuan Gu, Yanting Zheng, Yifan Wang, Jing Wu, Chunni Huang, Zhongqing Li, Jun Luo and 2 more

Abstract read
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Article in Blood and lymphatic cancer : targets and therapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

12 authors.

Yanyu Nong *Department of Clinical Laboratory, The First Affiliated Hospital of Guangxi Medical University, Key Laboratory of Clinical Laboratory Medicine of Guangxi Department of Education, Nanning, Guangxi, People's Republic of China.ORCID 0009-0002-4742-1614
Zengyi Xiong *Department of Clinical Laboratory, The First Affiliated Hospital of Guangxi Medical University, Key Laboratory of Clinical Laboratory Medicine of Guangxi Department of Education, Nanning, Guangxi, People's Republic of China.
Qicai Wang *Department of Clinical Laboratory, The First Affiliated Hospital of Guangxi Medical University, Key Laboratory of Clinical Laboratory Medicine of Guangxi Department of Education, Nanning, Guangxi, People's Republic of China.ORCID 0009-0005-3295-6458
Mengyuan GuDepartment of Clinical Laboratory, The First Affiliated Hospital of Guangxi Medical University, Key Laboratory of Clinical Laboratory Medicine of Guangxi Department of Education, Nanning, Guangxi, People's Republic of China.
Yanting ZhengDepartment of Clinical Laboratory, The First Affiliated Hospital of Guangxi Medical University, Key Laboratory of Clinical Laboratory Medicine of Guangxi Department of Education, Nanning, Guangxi, People's Republic of China.
Yifan WangDepartment of Clinical Laboratory, The First Affiliated Hospital of Guangxi Medical University, Key Laboratory of Clinical Laboratory Medicine of Guangxi Department of Education, Nanning, Guangxi, People's Republic of China.ORCID 0009-0006-5599-4753
Jing WuDepartment of Scientific Research, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, People's Republic of China.
Chunni HuangDepartment of Clinical Laboratory, The First Affiliated Hospital of Guangxi Medical University, Key Laboratory of Clinical Laboratory Medicine of Guangxi Department of Education, Nanning, Guangxi, People's Republic of China.
Zhongqing LiDepartment of Hematology, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, People's Republic of China.
Jun LuoDepartment of Hematology, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, People's Republic of China.
Zhian LingDepartment of Emergency, The Second Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, People's Republic of China.ORCID 0000-0001-7555-4460
Ruolin LiDepartment of Scientific Research, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, People's Republic of China.ORCID 0000-0002-9835-4987

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: BNIP3L regulates mitophagy and apoptosis, and its dysregulation is closely linked to the development and progression of cancers. Studies have shown that BNIP3L is valuable for assessing tumor progression and prognosis. This study aims to investigate the diagnostic and prognostic significance of serum BNIP3L levels in multiple myeloma (MM). Methods: The serum level of BNIP3L were measured in 152 MM patients and 158 healthy controls by Enzyme-Linked Immunosorbent Assay (ELISA). Receiver operating characteristic (ROC) curve analysis was performed to assess the diagnostic ability of MM. The prognostic relevance of serum BNIP3L levels in MM patients was assessed using Kaplan-Meier survival analysis and Cox regression. Results: Serum BNIP3L levels were significantly elevated in MM patients compared to healthy controls ( Conclusion: This study identified serum BNIP3L as a potential diagnostic biomarker for active MM. Elevated BNIP3L levels were significantly associated with adverse clinical characteristics, suboptimal treatment response, and a trend toward inferior survival. Consequently, measuring serum BNIP3L could be valuable for monitoring disease progression and prognostic evaluation in MM patients.

Indexed as

BNIP3Ldiagnosismultiple myelomaprognosisserum biomarker

Identifiers

PMID41439242
PMCPMC12719624

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