Evidence map›Paper›PMID 38956026›Full record

ArticleCell death & disease2024

RSL3 enhances ROS-mediated cell apoptosis of myelodysplastic syndrome cells through MYB/Bcl-2 signaling pathway.

Li Liu, Chaoying Yang, Lin Zhu, Yanyan Wang, Fuxiang Zheng, Long Liang, Pengfei Cao, Jing Liu, Xu Han, Ji Zhang

Abstract read
In one paragraph

Article in Cell death & disease, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. 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

10 authors.

Li Liu *Department of Clinical Laboratory, The Affiliated Nanhua Hospital, University of South China, Hengyang, 421001, Hunan, China.
Chaoying Yang *Molecular Biology Research Center & Center for Medical Genetics, School of Life Sciences, Central South University, Changsha, 410078, Hunan, China.
Lin Zhu *Department of Dermatology, Xiangya Hospital, Central South University, Changsha, 410078, Hunan, China.
Yanyan WangDepartment of Clinical Laboratory, The Affiliated Nanhua Hospital, University of South China, Hengyang, 421001, Hunan, China.
Fuxiang ZhengDepartment of Clinical Laboratory, Shenzhen Traditional Chinese Medicine Hospital, Shenzhen, 518033, Guangdong, China.
Long LiangMolecular Biology Research Center & Center for Medical Genetics, School of Life Sciences, Central South University, Changsha, 410078, Hunan, China.
Pengfei CaoDepartment of Hematology, Xiangya Hospital, Central South University, Changsha, 410078, Hunan, China.
Jing LiuMolecular Biology Research Center & Center for Medical Genetics, School of Life Sciences, Central South University, Changsha, 410078, Hunan, China.ORCID 0000-0001-5588-3865
Xu HanMolecular Biology Research Center & Center for Medical Genetics, School of Life Sciences, Central South University, Changsha, 410078, Hunan, China. hx1989345@163.com.ORCID 0000-0002-9317-774X
Ji ZhangDepartment of Clinical Laboratory, The Affiliated Nanhua Hospital, University of South China, Hengyang, 421001, Hunan, China. jizhang@fsyy.usc.edu.cn.ORCID 0000-0002-6610-9805

Funding

National Natural Science Foundation of China (National Science Foundation of China) 82370149,82170138 and 81870105
6 · The paper itself

Abstract

Myelodysplastic syndromes (MDS) are clonal hematopoietic malignancies and seriously threaten people's health. Current therapies include bone marrow transplantation and several hypomethylating agents. However, many elderly patients cannot benefit from bone marrow transplantation and many patients develop drug resistance to hypomethylating agents, making it urgent to explore novel therapy. RSL3 can effectively induce ferroptosis in various tumors and combination of RSL3 and hypomethylating agents is promising to treat many tumors. However, its effect in MDS was unknown. In this study, we found that RSL3 inhibited MDS cell proliferation through inducing ROS-dependent apoptosis. RSL3 inhibited Bcl-2 expression and increased caspase 3 and PARP cleavage. RNA-seq analysis revealed that MYB may be a potential target of RSL3. Rescue experiments showed that overexpression of MYB can rescue MDS cell proliferation inhibition caused by RSL3. Cellular thermal shift assay showed that RSL3 binds to MYB to exert its function. Furthermore, RSL3 inhibited tumor growth and decreased MYB and Bcl-2 expression in vivo. More importantly, RSL3 decreased the viability of bone marrow mononuclear cells (BMMCs) isolated from MDS patients, and RSL3 had a synergistic effect with DAC in MDS cells. Our studies have uncovered RSL3 as a promising compound and MYB/Bcl-2 signaling pathway as a potential target for MDS treatment.

Indexed as

ApoptosisMyelodysplastic SyndromesProto-Oncogene Proteins c-bcl-2Proto-Oncogene Proteins c-mybReactive Oxygen SpeciesSignal TransductionAnimalsCell ProliferationFemaleHumansMaleMiceMice, NudeBCL2 protein, humanMYB protein, humanProto-Oncogene Proteins c-bcl-2Proto-Oncogene Proteins c-mybReactive Oxygen Species

Identifiers

PMID38956026
PMCPMC11219730

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.