Evidence map›Paper›PMID 40058268›Full record

ArticleNeoplasia (New York, N.Y.)2025

HRP2 regulating MICU1-mediated Ca

Qian Li, Ziyi Peng, Li Lin, Zhiying Zhang, Jing Ma, Lin Chen, Su Liu, Shuang Gao, Linchuang Jia, Jingjing Wang and 4 more

Abstract read
In one paragraph

Article in Neoplasia (New York, N.Y.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Qian LiDepartment of Hematology, Tianjin Medical University Cancer Institute and Hospital; National Clinical Research Center of Cancer; Tianjin Key Laboratory of Cancer Prevention and Therapy; Tianjin's Clinical Research Center of Cancer, Tianjin, 300060 China.
Ziyi PengDepartment of Physiology and Pathophysiology, School of Basic Medical Science, Tianjin Medical University, Heping, Tianjin, 300070 China.
Li LinDepartment of Blood and Marrow Transplantation, Tianjin Cancer Hospital Airport Hospital, Tianjin 300308, China.
Zhiying ZhangDepartment of Blood and Marrow Transplantation, Tianjin Cancer Hospital Airport Hospital, Tianjin 300308, China.
Jing MaDepartment of Blood and Marrow Transplantation, Tianjin Cancer Hospital Airport Hospital, Tianjin 300308, China.
Lin ChenDepartment of Blood and Marrow Transplantation, Tianjin Cancer Hospital Airport Hospital, Tianjin 300308, China.
Su LiuDepartment of Blood and Marrow Transplantation, Tianjin Cancer Hospital Airport Hospital, Tianjin 300308, China.
Shuang GaoDepartment of Blood and Marrow Transplantation, Tianjin Cancer Hospital Airport Hospital, Tianjin 300308, China.
Linchuang JiaDepartment of Physiology and Pathophysiology, School of Basic Medical Science, Tianjin Medical University, Heping, Tianjin, 300070 China.
Jingjing WangShandong Provincial Key Laboratory of Precision Oncology, Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, 250117, China.
Zeng CaoDepartment of Hematology, Tianjin Medical University Cancer Institute and Hospital; National Clinical Research Center of Cancer; Tianjin Key Laboratory of Cancer Prevention and Therapy; Tianjin's Clinical Research Center of Cancer, Tianjin, 300060 China.
Xingli ZhaoDepartment of Hematology, Oncology Center, Tianjin Union Medical Center, Hongqiao, Tianjin, 300122, China. Electronic address: insectzhao@163.com.
Zhiqiang LiuShandong Provincial Key Laboratory of Precision Oncology, Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, 250117, China. Electronic address: zqliu@sdfmu.edu.cn.
Yafei WangDepartment of Hematology, Tianjin Medical University Cancer Institute and Hospital; National Clinical Research Center of Cancer; Tianjin Key Laboratory of Cancer Prevention and Therapy; Tianjin's Clinical Research Center of Cancer, Tianjin, 300060 China. Electronic address: yfwang@tmu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite the efficacy of bortezomib (BTZ)-based chemotherapy in treating multiple myeloma (MM) patients, chemoresistance occurs frequently over time, particularly in individuals exhibiting an initial positive response to BTZ therapy. In this study, we established BTZ-resistant MM cells and identified that suppressed expression of the hepatoma-derived growth factor (HDGF)-related protein-2 (HRP2) was a key determinant of chemoresistance in MM cells. Manipulating HRP2 expression remodeled the chemosensitivity of MM cells in vitro and in vivo. Clinically, lower expression of HRP2 predicted a shorter survival rate in MM patients receiving BTZ-based regimens. Mechanistically, HRP2 depletion resulted in elevated acetylation modifications of histone 3 at lysine 27 (H3K27Ac), and enhanced chromatin accessibility as well as transcriptional elongation of mitochondrial calcium uptake 1(MICU1) gene, thus promoting the expression of MICU1 gene and alleviating calcium (Ca

Indexed as

CalciumCalcium-Binding ProteinsDrug Resistance, NeoplasmMitochondrial Membrane Transport ProteinsMultiple MyelomaAnimalsAntineoplastic AgentsApoptosisBortezomibCation Transport ProteinsCell Line, TumorDisease Models, AnimalGene Expression Regulation, NeoplasticHumansMiceReactive Oxygen SpeciesAntineoplastic AgentsBortezomibCalciumCalcium-Binding ProteinsCation Transport ProteinsMICU1 protein, humanMitochondrial Membrane Transport ProteinsReactive Oxygen SpeciesCa(2+) overloadChemoresistanceHRP2MICU1Multiple myeloma

Identifiers

PMID40058268
PMCPMC11930454

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.