Evidence map›Paper›PMID 26701856›Full record

ArticleOncotarget2016

Fast clearance of lipid droplets through MAP1S-activated autophagy suppresses clear cell renal cell carcinomas and promotes patient survival.

Guibin Xu, Yaodong Jiang, Yuansong Xiao, Xian D Liu, Fei Yue, Wenjiao Li, Xun Li, Yongzhong He, Xianhan Jiang, Hai Huang and 3 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

37 citing papers in PubMed, 48 citations in OpenAlex.

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  12. Genes · 2023
    Article
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  16. Adaptive and maladaptive roles of lipid droplets in health and disease.American journal of physiology. Cell physiology · 2022
    Review
  17. Review
  18. Review
  19. An actin-WHAMM interaction linking SETD2 and autophagy.Biochemical and biophysical research communications · 2021
    Article
  20. 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

13 authors at 5 institutions in 2 countries.

Guibin XuDepartment of Urology, The Fifth Affiliated Hospital of Guangzhou Medical University, Guangzhou, Guangdong Province, 510700, China.
Yaodong JiangDepartment of Urology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong Province, 510515, China.
Yuansong XiaoDepartment of Urology, Guangzhou General Hospital of Guangzhou Military Command, Guangzhou, Guangdong Province, 510010, China.
Xian D LiuDepartment of Genitourinary Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, 77030, USA.
Fei YueInstitute of Biosciences and Technology, Texas A&M Health Science Center, Houston, Texas, 77030, USA.
Wenjiao LiInstitute of Biosciences and Technology, Texas A&M Health Science Center, Houston, Texas, 77030, USA.
Xun LiDepartment of Urology, The Fifth Affiliated Hospital of Guangzhou Medical University, Guangzhou, Guangdong Province, 510700, China.
Yongzhong HeDepartment of Urology, The Fifth Affiliated Hospital of Guangzhou Medical University, Guangzhou, Guangdong Province, 510700, China.
Xianhan JiangDepartment of Urology, The Fifth Affiliated Hospital of Guangzhou Medical University, Guangzhou, Guangdong Province, 510700, China.
Hai HuangInstitute of Biosciences and Technology, Texas A&M Health Science Center, Houston, Texas, 77030, USA.
Qi ChenInstitute of Biosciences and Technology, Texas A&M Health Science Center, Houston, Texas, 77030, USA.
Eric JonaschDepartment of Genitourinary Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, 77030, USA.
Leyuan LiuInstitute of Biosciences and Technology, Texas A&M Health Science Center, Houston, Texas, 77030, USA.
Texas A&M Health Science Center · USGuangzhou Medical University · CNThe University of Texas MD Anderson Cancer Center · USGeneral Hospital of Guangzhou Military Command · CNNanfang Hospital · CN

Funding

Roles of C19ORF5 and LRPPRC in Autophagy and Tumor SuppressionR01CA142862 · NCI · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI LIU, LEYUAN · 2010 to 2014
$1.2M
NCI NIH HHS 1R01CA142862NCI NIH HHS R01 CA142862
6 · The paper itself

Abstract

Clear cell renal cell carcinoma (ccRCC) is composed of cells whose cytoplasm filled with lipid droplets, subcellular organelles coated with adipocyte differentiation-related protein (ADFP) for the storage of triacylglycerol converted from excess free fatty acids. Mammalian cells primarily use the autophagy-lysosome system to degrade misfolded/aggregated proteins and dysfunctional organelles such as lipid droplets. MAP1S (originally named C19ORF5) is an autophagy activator and promotes the biogenesis and degradation of autophagosomes. Previously, we reported that MAP1S suppresses hepatocellular carcinogenesis in a mouse model and promoted the survival of patients with prostate adenocarcinomas by increasing the degradation of aggregated proteins and dysfunctional mitochondria. Here we show that a suppression of MAP1S in renal cells causes an impairment of autophagic clearance of lipid droplets. In contrast, an overexpression of MAP1S causes an activation of autophagy flux and a reduction of lipid droplets so less DNA double strand breakage is induced. The levels of MAP1S in normal renal cells are dramatically higher than those in the ccRCC tissues and cell lines derived from renal cell carcinomas. High levels of MAP1S are associated with a reduced malignancy and metastasis of ccRCC and predict a better survival of ccRCC patients. Therefore, autophagy defects in the degradation of lipid droplets triggered by the MAP1S deficiency may enhance the initiation and development of ccRCC and reduce the survival of ccRCC patients.

Indexed as

AnimalsAutophagyCarcinoma, Renal CellFemaleHumansKidney NeoplasmsLipid DropletsMaleMiceMicrotubule-Associated ProteinsMiddle AgedSurvival AnalysisMAP1S protein, humanMicrotubule-Associated ProteinsADFPccRCClipophagyMAP1Sprognosis

Identifiers

PMID26701856
PMCPMC4868754
OpenAlexW2218624552

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.