Evidence map›Paper›PMID 35449154›Full record

ArticleCell death discovery2022

ORP5 promotes tumor metastasis via stabilizing c-Met in renal cell carcinoma.

Li Song, Lin Zhang, Yun Zhou, Xiaotong Shao, Yuting Xu, Dongsheng Pei, Qingling Wang

Open access · goldAbstract read
In one paragraph

Article in Cell death discovery, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.7field-weighted citation impact, top 37% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Role of Oxysterol-Binding Protein Family in Cholesterol Metabolism and Cancer Progression: A Review.Medical science monitor : international medical journal of experimental and clinical research · 2026
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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

7 authors at 2 institutions in 1 country.

Li Song *Department of Pathology, Xuzhou Medical University, Xuzhou, Jiangsu, 221004, China.
Lin Zhang *Department of Pathology, Xuzhou Medical University, Xuzhou, Jiangsu, 221004, China.
Yun ZhouDepartment of Radiation Oncology, Xuzhou Central Hospital, Xuzhou, Jiangsu, 221000, China.
Xiaotong ShaoDepartment of Pathology, Xuzhou Medical University, Xuzhou, Jiangsu, 221004, China.
Yuting XuDepartment of Pathology, Xuzhou Medical University, Xuzhou, Jiangsu, 221004, China.
Dongsheng PeiDepartment of Pathology, Xuzhou Medical University, Xuzhou, Jiangsu, 221004, China. dspei@xzhmu.edu.cn.
Qingling WangDepartment of Pathology, Xuzhou Medical University, Xuzhou, Jiangsu, 221004, China. qlwang@xzhmu.edu.cn.ORCID http://orcid.org/0000-0002-0793-5808
Xuzhou Medical College · CNXuzhou Central Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

ORP5, a lipid transporter, has been reported to increase the metastasis of several cancers. However, the potential mechanisms of ORP5 in renal cell carcinoma (RCC) remain unclear. In this study, we demonstrated that ORP5 was commonly overexpressed in tumor cells and tissues of RCC, and associated with tumor progression. Overexpression of ORP5 could promote RCC cells migration and invasion. In addition, the results suggested that the expression of ORP5 was favorably associated with c-Met expression, and ORP5 promoted RCC cells metastasis by upregulating c-Met in vitro and in vivo. Mechanistically, ORP5 facilitated the ubiquitination and degradation of c-Cbl (the E3 ligase of c-Met), and thus inhibited c-Met lysosomal degradation, which resulted in the stabilization of c-Met. In general, these findings revealed the role of ORP5 in contributing to tumorigenesis via upregulating c-Met in RCC.

Identifiers

PMID35449154
PMCPMC9023482
OpenAlexW4224247715

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Registered trials

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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.