Evidence map›Paper›PMID 37689827›Full record

ArticleOncogene2023

Oncogenic BRAF noncanonically promotes tumor metastasis by mediating VASP phosphorylation and filopodia formation.

Wenting Pan, Yihao Tian, Qian Zheng, Zelin Yang, Yulong Qiang, Zun Zhang, Nan Zhang, Jie Xiong, Xin Zhu, Lei Wei and 1 more

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

5 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Colorectal cancer tumor phenotypes associated withWorld journal of gastrointestinal pathophysiology · 2025
    Article
  4. Article
  5. 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

11 authors at 2 institutions in 1 country.

Wenting PanDepartment of Pathology and Pathophysiology, School of Basic Medical Sciences, Wuhan University, Wuhan, China.
Yihao TianDepartment of Human Anatomy and Histology and Embryology, School of Basic Medical Sciences, Wuhan University, Wuhan, China.
Qian ZhengDepartment of Medical Genetics, School of Basic Medical Sciences, Wuhan University, Wuhan, China.
Zelin YangDepartment of Pathology and Pathophysiology, School of Basic Medical Sciences, Wuhan University, Wuhan, China.
Yulong QiangDepartment of Medical Genetics, School of Basic Medical Sciences, Wuhan University, Wuhan, China.
Zun ZhangDepartment of Gastrointestinal Surgery & Department of Gastric and Colorectal Surgical Oncology, Zhongnan Hospital of Wuhan University, Wuhan, China.
Nan ZhangDepartment of Medical Genetics, School of Basic Medical Sciences, Wuhan University, Wuhan, China.
Jie XiongDepartment of Immunology, School of Basic Medical Sciences, Wuhan University, Wuhan, China. jiexiong@whu.edu.cn.
Xin ZhuKey Laboratory of Head & Neck Cancer Translational Research of Zhejiang Province, Zhejiang Cancer Hospital, Hangzhou, China. zhuxin@zjcc.org.cn.
Lei WeiDepartment of Pathology and Pathophysiology, School of Basic Medical Sciences, Wuhan University, Wuhan, China. leiwei@whu.edu.cn.
Feng LiDepartment of Medical Genetics, School of Basic Medical Sciences, Wuhan University, Wuhan, China. fli222@whu.edu.cn.ORCID 0000-0002-9201-1668
Wuhan University · CNZhejiang Cancer Hospital · CN

Funding

National Natural Science Foundation of China (National Science Foundation of China) 82173137National Natural Science Foundation of China (National Science Foundation of China) 82373047
6 · The paper itself

Abstract

BRAF is frequently mutated in various cancer types and contributes to tumorigenesis and metastasis. As an important switch in RAS signaling pathway, BRAF typically enables the activation of MEK and ERK, and its mutation significantly promotes metastasis. However, whether BRAF could stimulate metastasis via a distinct manner is still unknown. Herein, we found that a portion of the BRAF protein localized at the plasma membrane and that the BRAF

Indexed as

Cell Adhesion MoleculesMicrofilament ProteinsPhosphoproteinsProto-Oncogene Proteins B-rafPseudopodiaAnimalsCell Line, TumorCell MovementFemaleHumansMiceMutationNeoplasm InvasivenessNeoplasm MetastasisPhosphorylationVasodilator-Stimulated PhosphoproteinBRAF protein, humanCell Adhesion MoleculesMicrofilament ProteinsPhosphoproteinsProto-Oncogene Proteins B-raf

Identifiers

PMID37689827
OpenAlexW4386569090

What OpenQuestion holds

Textmetadata
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.