Evidence map›Paper›PMID 39027150›Full record

ArticleCancer pathogenesis and therapy2024

Gene mutations in newly diagnosed multiple myeloma patients detected by next-generation sequencing technology.

Yutong Wang, Mengzhen Wang, Bin Chu, Minqiu Lu, Lei Shi, Shan Gao, Yuan Chen, Qin Yan, Na Ji, Li Bao

Erratum issuedAbstract read
In one paragraph

Article in Cancer pathogenesis and therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Knockdown of caspase-activated DNase and B-cell lymphoma 2 inhibits cell proliferation and drug resistance in TP53-mutant multiple myeloma.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Article
  4. Review
  5. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Yutong WangDepartment of Hematology, Beijing Jishuitan Hospital, Capital Medical University, Beijing 100035, China.
Mengzhen WangDepartment of Hematology, Beijing Jishuitan Hospital, Capital Medical University, Beijing 100035, China.
Bin ChuDepartment of Hematology, Beijing Jishuitan Hospital, Capital Medical University, Beijing 100035, China.
Minqiu LuDepartment of Hematology, Beijing Jishuitan Hospital, Capital Medical University, Beijing 100035, China.
Lei ShiDepartment of Hematology, Beijing Jishuitan Hospital, Capital Medical University, Beijing 100035, China.
Shan GaoDepartment of Hematology, Beijing Jishuitan Hospital, Capital Medical University, Beijing 100035, China.
Yuan ChenDepartment of Hematology, Beijing Jishuitan Hospital, Capital Medical University, Beijing 100035, China.
Qin YanDepartment of Hematology, Beijing Jishuitan Hospital, Capital Medical University, Beijing 100035, China.
Na JiDepartment of Hematology, Beijing Jishuitan Hospital, Capital Medical University, Beijing 100035, China.
Li BaoDepartment of Hematology, Beijing Jishuitan Hospital, Capital Medical University, Beijing 100035, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Multiple myeloma (MM) is a heterogeneous plasma-derived hematopoietic malignancy with complex genetic mutation contributing to the pathogenesis. Though gene sequencing has been applied in MM, genetic features from Chinese MM patients are reported less. We investigated the genetic mutation of newly diagnosed multiple myeloma (NDMM) patients and explore its correlation with cytogenetic abnormalities detected by fluorescence Methods: A total of 206 patients with NDMM were enrolled. After enriching plasma cells with CD138 magnetic beads, 92 MM-related target gene mutations were detected by the Illumina sequencing platform, and six common genetic abnormalities were detected by FISH. Results: 162 cases (78.6%) had at least one gene mutation detected by NDMM. The top 5 mutated genes were Conclusions: There are various gene mutations in NDMM patients, mainly

Indexed as

Genetics mutationMultiple myelomaNext-generation sequencing

Identifiers

PMID39027150
PMCPMC11252513

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