Evidence map›Paper›PMID 25469510›Full record

ArticlePloS one2014

GAIP interacting protein C-terminus regulates autophagy and exosome biogenesis of pancreatic cancer through metabolic pathways.

Santanu Bhattacharya, Krishnendu Pal, Anil K Sharma, Shamit K Dutta, Julie S Lau, Irene K Yan, Enfeng Wang, Ahmed Elkhanany, Khalid M Alkharfy, Arunik Sanyal and 4 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

52 citing papers in PubMed, 73 citations in OpenAlex.

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  15. Extracellular Vesicles as Mediators of Nickel-Induced Cancer Progression.International journal of molecular sciences · 2022
    Article
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  17. IMP1/IGF2BP1 in human colorectal cancer extracellular vesicles.American journal of physiology. Gastrointestinal and liver physiology · 2022
    Article
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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

14 authors at 3 institutions in 2 countries.

Santanu BhattacharyaDepartment Biochemistry and Molecular Biology, Mayo Clinic, Rochester, Minnesota, United States of America.
Krishnendu PalDepartment Biochemistry and Molecular Biology, Mayo Clinic, Rochester, Minnesota, United States of America.
Anil K SharmaDepartment Biochemistry and Molecular Biology, Mayo Clinic, Rochester, Minnesota, United States of America.
Shamit K DuttaDepartment Biochemistry and Molecular Biology, Mayo Clinic, Rochester, Minnesota, United States of America.
Julie S LauDepartment Biochemistry and Molecular Biology, Mayo Clinic, Rochester, Minnesota, United States of America.
Irene K YanDepartments of Transplantation and Cancer Biology, Mayo Clinic, Jacksonville, Florida, United States of America.
Enfeng WangDepartment Biochemistry and Molecular Biology, Mayo Clinic, Rochester, Minnesota, United States of America.
Ahmed ElkhananyDepartment Biochemistry and Molecular Biology, Mayo Clinic, Rochester, Minnesota, United States of America.
Khalid M AlkharfyDepartment Biochemistry and Molecular Biology, Mayo Clinic, Rochester, Minnesota, United States of America; Department of Pharmacy, King Saud University, Riyadh, Saudi Arabia.
Arunik SanyalDepartment Biochemistry and Molecular Biology, Mayo Clinic, Rochester, Minnesota, United States of America.
Tushar C PatelDepartments of Transplantation and Cancer Biology, Mayo Clinic, Jacksonville, Florida, United States of America.
Suresh T ChariDepartment of Internal Medicine, Mayo Clinic, Rochester, Minnesota, United States of America.
Mark R SpallerDepartment of Pharmacology and Toxicology, Geisel School of Medicine at Dartmouth, and Norris Cotton Cancer Center, Lebanon, New Hampshire, United States of America.
Debabrata MukhopadhyayDepartment Biochemistry and Molecular Biology, Mayo Clinic, Rochester, Minnesota, United States of America.
Mayo Clinic · USMayo Clinic in Florida · USDartmouth College · US

Funding

Targeting Pancreatic Cancer Using Peptide Chemistry: From Bench to BedsideR01CA150190 · NCI · MAYO CLINIC ROCHESTER · PI MIERKE, DALE F, MUKHOPADHYAY, DEBABRATA · 2010 to 2021
$5.7M
Regulatory Pathways and Role of VPF/VEGF in Renal CancerR01CA078383 · NCI · MAYO CLINIC ROCHESTER · PI MUKHOPADHYAY, DEBABRATA · 2004 to 2019
$4.5M
Mechanisms of Survival Signaling in Biliary EpitheliaR01DK069370 · NIDDK · SCOTT AND WHITE MEMORIAL HOSPITAL · PI PATEL, TUSHAR · 2005 to 2014
$2.4M
Extracellular non-coding RNA biomarkers of hepatocellular cancerUH2TR000884 · NCATS · MAYO CLINIC JACKSONVILLE · PI PATEL, TUSHAR · 2013 to 2014
$989k
REGULATORY PATHWAYS AND ROLE OF VPF/VEGF IN RENAL CANCERR29CA078383 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI MUKHOPADHYAY, DEBABRATA · 1998 to 2002
$383k
NCATS NIH HHS UH2 TR000884NCI NIH HHS CA150190NCI NIH HHS CA78383NCI NIH HHS R01 CA078383NCI NIH HHS R01 CA150190NCI NIH HHS R29 CA078383NIDDK NIH HHS R01 DK069370
6 · The paper itself

Abstract

GAIP interacting protein C terminus (GIPC) is known to play an important role in a variety of physiological and disease states. In the present study, we have identified a novel role for GIPC as a master regulator of autophagy and the exocytotic pathways in cancer. We show that depletion of GIPC-induced autophagy in pancreatic cancer cells, as evident from the upregulation of the autophagy marker LC3II. We further report that GIPC regulates cellular trafficking pathways by modulating the secretion, biogenesis, and molecular composition of exosomes. We also identified the involvement of GIPC on metabolic stress pathways regulating autophagy and microvesicular shedding, and observed that GIPC status determines the loading of cellular cargo in the exosome. Furthermore, we have shown the overexpression of the drug resistance gene ABCG2 in exosomes from GIPC-depleted pancreatic cancer cells. We also demonstrated that depletion of GIPC from cancer cells sensitized them to gemcitabine treatment, an avenue that can be explored as a potential therapeutic strategy to overcome drug resistance in cancer.

Indexed as

AutophagyAdaptor Proteins, Signal TransducingAntimetabolites, AntineoplasticApoptosis Regulatory ProteinsATP-Binding Cassette TransportersATP Binding Cassette Transporter, Subfamily G, Member 2Autophagy-Related Protein 7Beclin-1Biological TransportCell Line, TumorDeoxycytidineDrug Resistance, NeoplasmExosomesGemcitabineGene ExpressionGlucoseABCG2 protein, humanAdaptor Proteins, Signal TransducingAntimetabolites, AntineoplasticApoptosis Regulatory ProteinsATG7 protein, humanATP-Binding Cassette TransportersATP Binding Cassette Transporter, Subfamily G, Member 2Autophagy-Related Protein 7Beclin-1BECN1 protein, humanDeoxycytidineGemcitabineGIPC1 protein, humanGlucoseMembrane ProteinsNeoplasm ProteinsUbiquitin-Activating Enzymes

Identifiers

PMID25469510
PMCPMC4255029
OpenAlexW2089605985

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.