Evidence map›Paper›PMID 35912545›Full record

ArticleCancer science2022

MYO10 contributes to the malignant phenotypes of colorectal cancer via RACK1 by activating integrin/Src/FAK signaling.

Haibin Ou, Lili Wang, Ziyao Xi, Hui Shen, Yaofei Jiang, Fuxiang Zhou, Yu Liu, Yunfeng Zhou

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 12% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Pooled it
  2. Emerging Roles of Cytoneme-Mediated Signaling in Cancer.International journal of molecular sciences · 2026
    Review
  3. Article
  4. Article
  5. Article
  6. Magnesium cantharidate inhibits hepatocellular cancer by targeting RACK1.American journal of translational research · 2025
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
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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 at 1 institution in 1 country.

Haibin OuDepartment of Radiation and Medical Oncology, Zhongnan Hospital, Wuhan University, Wuhan, China.ORCID https://orcid.org/0000-0003-3208-3632
Lili WangDepartment of Radiation and Medical Oncology, Zhongnan Hospital, Wuhan University, Wuhan, China.
Ziyao XiDepartment of Radiation and Medical Oncology, Zhongnan Hospital, Wuhan University, Wuhan, China.
Hui ShenDepartment of Radiation and Medical Oncology, Zhongnan Hospital, Wuhan University, Wuhan, China.
Yaofei JiangDepartment of Radiation and Medical Oncology, Zhongnan Hospital, Wuhan University, Wuhan, China.
Fuxiang ZhouDepartment of Radiation and Medical Oncology, Zhongnan Hospital, Wuhan University, Wuhan, China.ORCID https://orcid.org/0000-0001-9216-5395
Yu LiuDepartment of Radiation and Medical Oncology, Zhongnan Hospital, Wuhan University, Wuhan, China.
Yunfeng ZhouDepartment of Radiation and Medical Oncology, Zhongnan Hospital, Wuhan University, Wuhan, China.ORCID https://orcid.org/0000-0003-4328-6646
Wuhan University · CN

Funding

National Natural Science Foundation of China 81370070National Natural Science Foundation of China 81472799
6 · The paper itself

Abstract

Liver metastases still remain a major cause of colorectal cancer (CRC) patient death. MYO10 is upregulated in several tumor types; however, its significance and the underlying mechanism in CRC are not entirely clear. Here, we found that MYO10 was highly expressed in CRC tumor tissues, especially in liver metastasis tissues. MYO10 knockout reduced CRC cell proliferation, invasion, and migration in vitro and CRC metastasis in vivo. We identified RACK1 by LC-MS/MS and demonstrated that MYO10 interacts with and stabilizes RACK1. Mechanistically, MYO10 promotes CRC cell progression and metastasis via ubiquitination-mediated RACK1 degradation and integrin/Src/FAK signaling activation. Therefore, the MYO10/RACK1/integrin/Src/FAK axis may play an important role in CRC progression and metastasis.

Indexed as

Colorectal NeoplasmsLiver NeoplasmsMyosinsAnimalsCell Line, TumorCell MovementCell ProliferationChromatography, LiquidHumansIntegrinsNeoplasm ProteinsPhenotypeReceptors for Activated C KinaseTandem Mass SpectrometryIntegrinsMYO10 protein, humanMyosinsNeoplasm ProteinsRACK1 protein, humanReceptors for Activated C Kinasecolorectal cancerintegrin/Src/FAK signalingMYO10RACK1tumorigenesis

Identifiers

PMID35912545
PMCPMC9633311
OpenAlexW4289337681

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.