Evidence map›Paper›PMID 35071234›Full record

ArticleFrontiers in cell and developmental biology2021

Single-Cell Transcriptomes Combining with Consecutive Genomics Reveal Clonal Evolution and Gene Regulatory Networks in Relapsed and Refractory Multiple Myeloma.

Jiadai Xu, Yue Wang, Zheng Wei, Jingli Zhuang, Jing Li, Yifeng Sun, Liang Ren, Yawen Wang, Panpan Li, Shiyang Gu and 5 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.0field-weighted citation impact, top 25% of its field
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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
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

15 authors at 4 institutions in 1 country.

Jiadai XuDepartment of Hematology, Zhongshan Hospital, Fudan University, Shanghai, China.
Yue WangDepartment of Hematology, Zhongshan Hospital, Fudan University, Shanghai, China.
Zheng WeiDepartment of Hematology, Zhongshan Hospital, Fudan University, Shanghai, China.
Jingli ZhuangDepartment of Hematology, Zhongshan Hospital, Fudan University, Shanghai, China.
Jing LiDepartment of Hematology, Zhongshan Hospital, Fudan University, Shanghai, China.
Yifeng SunDepartment of Hematology, Zhongshan Hospital, Fudan University, Shanghai, China.
Liang RenDepartment of Hematology, Zhongshan Hospital, Fudan University, Shanghai, China.
Yawen WangDepartment of Hematology, Zhongshan Hospital, Fudan University, Shanghai, China.
Panpan LiDepartment of Hematology, Zhongshan Hospital, Fudan University, Shanghai, China.
Shiyang GuDepartment of Hematology, Zhongshan Hospital, Fudan University, Shanghai, China.
Yian ZhangDepartment of Hematology, Zhongshan Hospital, Fudan University, Shanghai, China.
Jifeng JiangDepartment of Hematology, Zhongshan Hospital, Fudan University, Shanghai, China.
Chen ChenDepartment of Hematology, Zhongshan Hospital, Fudan University, Shanghai, China.
Yu ZhangDepartment of Cardiovascular Surgery, Renji Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, China.
Peng LiuDepartment of Hematology, Zhongshan Hospital, Fudan University, Shanghai, China.
Fudan University · CNThe First Affiliated Hospital, Sun Yat-sen University · CNSun Yat-sen University · CNZhongshan Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study attempted to investigate how clonal structure evolves, along with potential regulatory networks, as a result of multiline therapies in relapsed/refractory multiple myeloma (RRMM). Eight whole exome sequencing (WES) and one single cell RNA sequencing (scRNA-seq) were performed in order to assess dynamic genomic changes in temporal consecutive samples of one RRMM patient from the time of diagnosis to death (about 37 months). The 63-year-old female patient who suffered from MM (P1) had disease progression (PD) nine times from July 2017 [newly diagnosed (ND)] to Aug 2020 (death), and the force to drive branching-pattern evolution of malignant PCs was found to be sustained. The mutant-allele tumor heterogeneity (MATH) and tumor mutation burden (TMB) initially exhibited a downward trend, which was then upward throughout the course of the disease. Various somatic single nucleotide variants (SNVs) that had disappeared after the previous treatment were observed to reappear in later stages. Chromosomal instability (CIN) and homologous recombination deficiency (HRD) scores were observed to be increased during periods of all progression, especially in the period of extramedullary plasmacytoma. Finally, in combination with WES and scRNA-seq of P1-PD9 (the nineth PD), the intro-heterogeneity and gene regulatory networks of MM cells were deciphered. As verified by the overall survival of MM patients in the MMRF CoMMpass and GSE24080 datasets, RUNX3 was identified as a potential driver for RRMM.

Indexed as

clonal evolutionheterogeneitymultiple myelomarefractoryrelapsed

Identifiers

PMID35071234
PMCPMC8766805
OpenAlexW4205976679

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.