Evidence map›Paper›PMID 40173324›Full record

ArticleAging2025

Comprehensive genomic characterization of programmed cell death-related genes to predict drug resistance and prognosis for patients with multiple myeloma.

Yan Li, Fuxu Wang, Hongbo Zhao, Zhenwei Jia, Xiaoyan Liu, Guirong Cui, Tiejun Qin, Xiaoyang Kong

Abstract read
In one paragraph

Article in Aging, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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

What it found

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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

1 citing paper in PubMed.

  1. Programmed cell death in lung cancer: mechanisms, immune responses, and therapeutics.Apoptosis : an international journal on programmed cell death · 2026
    Review
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

8 authors.

Yan LiHematology Department, Handan First Hospital, Handan 056001, China.
Fuxu WangDepartment of Hematology, Key Laboratory of Hematology of Hebei Province, Second Hospital of Hebei Medical University, Shijiazhuang 050000, China.
Hongbo ZhaoHematology Department, Handan First Hospital, Handan 056001, China.
Zhenwei JiaHematology Department, Handan First Hospital, Handan 056001, China.
Xiaoyan LiuHematology Department, Handan First Hospital, Handan 056001, China.
Guirong CuiHematology Department, Handan First Hospital, Handan 056001, China.
Tiejun QinMDS and MPN Centre, Institute of Haematology and Blood Diseases Hospital, Tianjin 300020, China.
Xiaoyang KongHematology Department, Handan First Hospital, Handan 056001, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMultiple myeloma (MM) is a cancer that is difficult to be diagnosed and treated. This study aimed to identify programmed cell death (PCD)-related molecular subtypes of MM and to assess their impact on patients' prognosis, immune status, and drug sensitivity.

methodsWe used the ConsensusClusterPlus method to classify molecular subtypes with prognostically relevant PCD genes from the MM patients screened. A prognostic model and a nomogram were established applying one-way COX regression analysis and LASSO Cox regression analysis. MM patients' sensitivity to chemotherapeutic agents was predicted for at-risk populations.

resultsSix molecular subtypes were classified employing PCD-related genes, notably, three of them had a higher tendency for immune escape and two of them were correlated with a worse prognosis of MM. Furthermore, the C3 subtype had activated pathways such as oxidative phosphorylation and DNA repair, while the C2 and C4 subtypes had activated pathways related to apoptosis. The Risk score showed that the nomogram can correctly predict the OS for MM patients, in particular, patients in the high-risk group had low overall survival (OS). Pharmacovigilance analyses revealed that patients in the high-risk and low-risk groups had greater IC

conclusionsA 12-gene Risk score model developed with PCD-related genes can accurately predict the survival for MM patients. Our study provided potential targets and strategies for individualized treatment of MM.

Indexed as

ApoptosisDrug Resistance, NeoplasmMultiple MyelomaAgedAntineoplastic AgentsFemaleGenomicsHumansMaleMiddle AgedNomogramsPrognosisAntineoplastic Agentsdrug sensitivityimmune statusmolecular subtypesmultiple myelomaprogrammed cell death

Identifiers

PMID40173324
PMCPMC12074814

What OpenQuestion holds

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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.