Evidence map›Paper›PMID 30836712›Full record

ArticleCancers2019

Ghrelin Upregulates Oncogenic Aurora A to Promote Renal Cell Carcinoma Invasion.

Tsung-Chieh Lin, Yuan-Ming Yeh, Wen-Lang Fan, Yu-Chan Chang, Wei-Ming Lin, Tse-Yen Yang, Michael Hsiao

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

8 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Matrix Metalloproteinase-10 in Kidney Injury Repair and Disease.International journal of molecular sciences · 2022
    Review
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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 5 institutions in 1 country.

Tsung-Chieh LinGenomic Medicine Core Laboratory, Chang Gung Memorial Hospital, Linkou 33305, Taiwan. tclin1980@gmail.com.ORCID 0000-0002-5985-3580
Yuan-Ming YehGenomic Medicine Core Laboratory, Chang Gung Memorial Hospital, Linkou 33305, Taiwan. yeh234@gmail.com.ORCID 0000-0001-8720-947X
Wen-Lang FanGenomic Medicine Core Laboratory, Chang Gung Memorial Hospital, Linkou 33305, Taiwan. alangfan@gmail.com.
Yu-Chan ChangGenomics Research Center, Academia Sinica, Taipei 11529, Taiwan. jameskobe0@gmail.com.
Wei-Ming LinDepartment of Diagnostic Radiology, Chang Gung Memorial Hospital, Chiayi Branch, Chang Gung University of Science and Technology, Chiayi 61363, Taiwan. weiming276@gmail.com.
Tse-Yen YangDepartment of Medical Research, China Medical University Hospital, China Medical University, Taichung 40447, Taiwan. hardawayoung@gmail.com.ORCID 0000-0002-3165-132X
Michael HsiaoGenomics Research Center, Academia Sinica, Taipei 11529, Taiwan. mhsiao@gate.sinica.edu.tw.ORCID 0000-0001-8529-9213
Chang Gung Memorial Hospital · TWChang Gung University of Science and Technology · TWChina Medical University · TWGenomics Research Center, Academia Sinica · TWKaohsiung Medical University · TW

Funding

Chang Gung Memorial Hospital, Linkou CMRPG3G0612Ministry of Science and Technology, Taiwan MOST 106-0210-01-15-02, MOST 107-0210-01-19-01, MOST 106-2314-B-182A-004 -MY2, MOST 107-2314-B-182A-158 -MY3
6 · The paper itself

Abstract

Ghrelin is a peptide hormone, originally identified from the stomach, that functions as an endogenous ligand of the growth hormone secretagogue receptor (GHSR) and promotes growth hormone (GH) release and food intake. Increasing reports point out ghrelin's role in cancer progression. We previously characterized ghrelin's prognostic significance in the clear cell subtype of renal cell carcinoma (ccRCC), and its pro-metastatic ability via Snail-dependent cell migration. However, ghrelin's activity in promoting cell invasion remains obscure. In this study, an Ingenuity Pathway Analysis (IPA)-based investigation of differentially expressed genes in Cancer Cell Line Encyclopedia (CCLE) dataset indicated the potential association of Aurora A with ghrelin in ccRCC metastasis. In addition, a significant correlation between ghrelin and Aurora A expression level in 15 ccRCC cell line was confirmed by variant probes. ccRCC patients with high ghrelin and Aurora A status were clinically associated with poor outcome. We further observed that ghrelin upregulated Aurora A at the protein and RNA levels and that ghrelin-induced ccRCC in vitro invasion and in vivo metastasis occurred in an Aurora A-dependent manner. Furthermore, MMP1, 2, 9 and 10 expressions are associated with poor outcome. In particular, MMP10 is significantly upregulated and required for the ghrelin-Aurora A axis to promote ccRCC invasion. The results of this study indicated a novel signaling mechanism in ccRCC metastasis.

Indexed as

aurora AghrelininvasionMMP10

Identifiers

PMID30836712
PMCPMC6468656
OpenAlexW2920688707

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.