Evidence map›Paper›PMID 29572236›Full record

ArticleCancer discovery2018

PTEN Deficiency and AMPK Activation Promote Nutrient Scavenging and Anabolism in Prostate Cancer Cells.

Seong M Kim, Tricia T Nguyen, Archna Ravi, Peter Kubiniok, Brendan T Finicle, Vaishali Jayashankar, Leonel Malacrida, Jue Hou, Jane Robertson, Dong Gao and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer discovery, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 125 papers.

0numbers the graph read from it
0cells of the map it votes in
125citing papers in PubMed
8.0field-weighted citation impact, top 2% 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

125 citing papers in PubMed, 194 citations in OpenAlex.

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  18. Review
  19. Oncogenic Control of Metabolism.Cold Spring Harbor perspectives in medicine · 2024
    Review
  20. Growth Signaling Networks Orchestrate Cancer Metabolic Networks.Cold Spring Harbor perspectives in medicine · 2024
    Review

65 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 5 institutions in 3 countries.

Seong M Kim *Department of Developmental and Cell Biology, University of California, Irvine, California.
Tricia T Nguyen *Department of Developmental and Cell Biology, University of California, Irvine, California.
Archna Ravi *Department of Developmental and Cell Biology, University of California, Irvine, California.
Peter KubiniokDepartment of Chemistry, Université de Montréal, Quebec, Canada.
Brendan T FinicleDepartment of Developmental and Cell Biology, University of California, Irvine, California.
Vaishali JayashankarDepartment of Developmental and Cell Biology, University of California, Irvine, California.
Leonel MalacridaLaboratory for Fluorescence Dynamics, University of California, Irvine, California.
Jue HouLaser Microbeam and Medical Program, Beckman Laser Institute and Medical Clinic, University of California, Irvine, California.
Jane RobertsonDepartment of Developmental and Cell Biology, University of California, Irvine, California.
Dong GaoKey Laboratory of Systems Biology, Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai, China.
Jonathan ChernoffCancer Biology Program, Fox Chase Cancer Center, Philadelphia, Pennsylvania.
Michelle A DigmanLaboratory for Fluorescence Dynamics, University of California, Irvine, California.
Eric O PotmaLaser Microbeam and Medical Program, Beckman Laser Institute and Medical Clinic, University of California, Irvine, California.
Bruce J TrombergLaser Microbeam and Medical Program, Beckman Laser Institute and Medical Clinic, University of California, Irvine, California.
Pierre ThibaultDepartment of Chemistry, Université de Montréal, Quebec, Canada.
Aimee L EdingerDepartment of Developmental and Cell Biology, University of California, Irvine, California. aedinger@uci.edu.
University of California, Irvine · USUniversité de Montréal · CAChinese Academy of Sciences · CNFluor (United States) · USFox Chase Cancer Center · US

Funding

Univ.of Calif., Irvine Cancer Center Support GrantP30CA062203 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI Christine Hui · 1994 to 2026
$57.9M
Uncover Strategies Used By Biological SystemsP50GM076516 · NIGMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI LANDER, ARTHUR D · 2007 to 2016
$25.1M
YEAST RIBOSOMAL STALK COMPOSITION IN VIVO BY TWO-PHOTON FCS AND PCH ANALYSISP41RR003155 · NCRR · UNIVERSITY OF ILLINOIS URBANA-CHAMPAIGN · PI GRATTON, ENRICO · 1986 to 2011
$14.9M
TRD4: Phasor analysisP41GM103540 · NIGMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI GRATTON, ENRICO · 2012 to 2020
$12.5M
Virtual Photonocs TechnologiesP41EB015890 · NIBIB · UNIVERSITY OF CALIFORNIA-IRVINE · PI DURKIN, ANTHONY · 2012 to 2017
$7.0M
Effects of sphingolipids on nutrient transporter expression and bioenergeticsR01GM089919 · NIGMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI EDINGER, AIMEE L · 2010 to 2014
$1.5M
NCI NIH HHS P30 CA062203NCRR NIH HHS P41 RR003155NIBIB NIH HHS P41 EB015890NIGMS NIH HHS P41 GM103540NIGMS NIH HHS P50 GM076516NIGMS NIH HHS R01 GM089919
6 · The paper itself

Abstract

We report that PTEN-deficient prostate cancer cells use macropinocytosis to survive and proliferate under nutrient stress. PTEN loss increased macropinocytosis only in the context of AMPK activation, revealing a general requirement for AMPK in macropinocytosis and a novel mechanism by which AMPK promotes survival under stress. In prostate cancer cells, albumin uptake did not require macropinocytosis, but necrotic cell debris proved a specific macropinocytic cargo. Isotopic labeling confirmed that macropinocytosed necrotic cell proteins fueled new protein synthesis in prostate cancer cells. Supplementation with necrotic debris, but not albumin, also maintained lipid stores, suggesting that macropinocytosis can supply nutrients other than amino acids. Nontransformed prostatic epithelial cells were not macropinocytic, but patient-derived prostate cancer organoids and xenografts and autochthonous prostate tumors all exhibited constitutive macropinocytosis, and blocking macropinocytosis limited prostate tumor growth. Macropinocytosis of extracellular material by prostate cancer cells is a previously unappreciated tumor-microenvironment interaction that could be targeted therapeutically.

Indexed as

PinocytosisStress, PhysiologicalAMP-Activated Protein KinasesAnimalsGene DeletionHumansMaleMiceMice, Inbred C57BLNutrientsProstatic NeoplasmsPTEN PhosphohydrolaseAMP-Activated Protein KinasesNutrientsPTEN Phosphohydrolase

Identifiers

PMID29572236
PMCPMC6030497
OpenAlexW2789786349

What OpenQuestion holds

Textmetadata
LicenceTDM
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.