Evidence map›Paper›PMID 36453019›Full record

ArticleMolecular oncology2023

Ryanodine receptor 2 promotes colorectal cancer metastasis by the ROS/BACH1 axis.

Tianwei Chen, Xilin Zhang, Xufen Ding, Jing Feng, Xueli Zhang, Dong Xie, Xiang Wang

Open access · goldAbstract read
In one paragraph

Article in Molecular oncology, 2023. 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
1.2field-weighted citation impact, top 22% 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

12 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. S-acylation of CaChronic diseases and translational medicine · 2024
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. 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

7 authors at 4 institutions in 1 country.

Tianwei ChenKey Laboratory of Integrated Oncology and Intelligent Medicine of Zhejiang Province, Department of Hepatobiliary and Pancreatic Surgery, Affiliated Hangzhou First People's Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Xilin ZhangDepartment of Central Laboratory, First Affiliated Hospital of Huzhou University, China.
Xufen DingCAS Key Laboratory of Nutrition, Metabolism and Food Safety, Shanghai Institute of Nutrition and Health, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai, China.
Jing FengDepartment of General Surgery, Fengxian Hospital Affiliated to Southern Medical University, Shanghai, China.
Xueli ZhangDepartment of General Surgery, Fengxian Hospital Affiliated to Southern Medical University, Shanghai, China.
Dong XieCAS Key Laboratory of Nutrition, Metabolism and Food Safety, Shanghai Institute of Nutrition and Health, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai, China.
Xiang WangKey Laboratory of Integrated Oncology and Intelligent Medicine of Zhejiang Province, Department of Hepatobiliary and Pancreatic Surgery, Affiliated Hangzhou First People's Hospital, Zhejiang University School of Medicine, Hangzhou, China.ORCID 0000-0003-0440-6203
Huzhou University · CNHangzhou First People's Hospital · CNShanghai Institute of Nutrition and Health · CNSouthern Medical University · CN

Funding

China Postdoctoral Science FoundationHuzhou Science and Technology Fund 2018GY04National Natural Science Foundation of China 81870377National Natural Science Foundation of China 81970570National Natural Science Foundation of China 82003076National Natural Science Foundation of China 82172361Shanghai Super Postdoctoral Program and Special Research Assistant of Chinese Academy of Sciences
6 · The paper itself

Abstract

There is no targeted therapy for KRAS proto-oncogene, GTPase (KRAS)-mutant metastatic colorectal cancer (mCRC) because the underlying mechanism remains obscure. Based on bioinformatic analysis, this study aims to elucidate a potential gene target for which an approved drug is available, and to reveal the function as well as the underlying mechanism of the candidate gene. Here, we identified that ryanodine receptor 2 (RyR2) expression was upregulated in KRAS-mutant mCRC, and that this promoted cancer cell metastasis. S107, an approved drug to inhibit calcium release from RyR2 in the clinic, inhibited cancer cell metastasis both in vitro and in vivo. High expression of RyR2 predicts poor survival in our patient cohort. CRC patients with serosa invasion and vascular tumor thrombus are characterized by high RyR2 expression. Analysis of expression profiles upon RyR2 knockdown and inhibition, revealed a set of metastasis-related molecules, and identified BTB domain and CNC homolog 1 (BACH1) as the main transcription factor regulated by RyR2. RyR2 regulates cellular reactive oxygen species (ROS) levels, which activates nuclear factor erythroid 2-related factor 2 (Nrf2; also known as NFE2L2) and HMOX1 expression, and thus BACH1 accumulation. Collectively, this study provides evidence that the RyR2/ROS/BACH1 axis may be a potential intervention target for CRC metastasis.

Indexed as

Basic-Leucine Zipper Transcription FactorsColonic NeoplasmsColorectal NeoplasmsBTB-POZ DomainHumansNeoplasm MetastasisNF-E2-Related Factor 2Proto-Oncogene Proteins p21(ras)Reactive Oxygen SpeciesRyanodine Receptor Calcium Release ChannelBACH1 protein, humanBasic-Leucine Zipper Transcription FactorsNF-E2-Related Factor 2Proto-Oncogene Proteins p21(ras)Reactive Oxygen SpeciesRyanodine Receptor Calcium Release Channelcolorectal cancermetastasisROSRyR2

Identifiers

PMID36453019
PMCPMC10061290
OpenAlexW4310572294

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.