Evidence map›Paper›PMID 34249081›Full record

ArticleFrontiers in genetics2021

Downregulated F-Box/LRR-Repeat Protein 7 Facilitates Pancreatic Cancer Metastasis by Regulating Snail1 for Proteasomal Degradation.

Liang Tang, Meng Ji, Xing Liang, Danlei Chen, Anan Liu, Guang Yang, Ligang Shi, Zhiping Fu, Chenghao Shao

Open access · goldAbstract read
In one paragraph

Article in Frontiers in genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 42% 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

4 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. 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

9 authors at 1 institution in 1 country.

Liang TangDepartment of Pancreatic-Biliary Surgery, Changzheng Hospital, Second Military Medical University, Shanghai, China.
Meng JiDepartment of Pancreatic-Biliary Surgery, Changzheng Hospital, Second Military Medical University, Shanghai, China.
Xing LiangDepartment of Pancreatic-Biliary Surgery, Changzheng Hospital, Second Military Medical University, Shanghai, China.
Danlei ChenDepartment of Pancreatic-Biliary Surgery, Changzheng Hospital, Second Military Medical University, Shanghai, China.
Anan LiuDepartment of Pancreatic-Biliary Surgery, Changzheng Hospital, Second Military Medical University, Shanghai, China.
Guang YangDepartment of Pancreatic-Biliary Surgery, Changzheng Hospital, Second Military Medical University, Shanghai, China.
Ligang ShiDepartment of Pancreatic-Biliary Surgery, Changzheng Hospital, Second Military Medical University, Shanghai, China.
Zhiping FuDepartment of Pancreatic-Biliary Surgery, Changzheng Hospital, Second Military Medical University, Shanghai, China.
Chenghao ShaoDepartment of Pancreatic-Biliary Surgery, Changzheng Hospital, Second Military Medical University, Shanghai, China.
Second Military Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pancreatic cancer (PCa) is one of the most aggressive lethal malignancies, and cancer metastasis is the major cause of PCa-associated death. F-box/LRR-repeat protein 7 (FBXL7) regulates cancer metastasis and the chemosensitivity of human pancreatic cancer. However, the clinical significance and biological role of FBXL7 in PCa have been rarely studied. In this study, we found that the expression of FBXL7 was down-regulated in PCa tissues compared with tumor-adjacent tissues, and the low expression of FBXL7 was positively associated with cancer metastasis. Functionally, overexpression of FBXL7 attenuated PANC1 cell invasion, whereas FBXL7 silencing promoted BxPC-3 cell invasion. Forced expression of FBXL7 upregulated the expression of epithelial markers (e.g., E-cadherin) and repressed the expression of mesenchymal markers (e.g., N-cadherin and Vimentin), indicating that FBXL7 negatively regulated the epithelial-mesenchymal transition (EMT) of PCa cells. Furthermore, we identified that FBXL7 repressed the expression of Snail1, a crucial transcription factor of EMT. Mechanistically, FBXL7 bound to Snail1 and promoted its ubiquitination and proteasomal degradation.

Indexed as

BxPC-3 cellEMTFBXL7pancreatic cancerSnail1

Identifiers

PMID34249081
PMCPMC8264591
OpenAlexW3175565016

What Socratic 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 Socratic graph.