Evidence map›Paper›PMID 38253423›Full record

ReviewCold Spring Harbor perspectives in medicine2024

Role of Tumor Cell Intrinsic and Host Autophagy in Cancer.

Jessie Yanxiang Guo, Eileen White

Abstract readReview
In one paragraph

Review in Cold Spring Harbor perspectives in medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
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

10 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. The authors respond to feedback onFrontiers in oncology · 2026
    Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. 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

2 authors at 1 institution in 1 country.

Jessie Yanxiang GuoRutgers Cancer Institute of New Jersey, New Brunswick, New Jersey 08903, USA.
Eileen WhiteRutgers Cancer Institute of New Jersey, New Brunswick, New Jersey 08903, USA epwhite@cinj.rutgers.edu.
Ludwig Cancer Research · US

Funding

Tumor cell metabolism in actionR01CA163591 · NCI · RUTGERS, THE STATE UNIV OF N.J. · PI JOSHUA D RABINOWITZ, Eileen P. White · 2012 to 2026
$7.0M
CANCAN-RUTGERSOT2CA278609 · NCI · RUTGERS BIOMEDICAL AND HEALTH SCIENCES · PI Eileen P. White · 2022 to 2026
$2.6M
Elucidate the mechanism of autophagy in supporting Lkb1-deficient lung tumorigenesis and metastasisR01CA237347 · NCI · RUTGERS BIOMEDICAL AND HEALTH SCIENCES · PI GUO, YANXIANG · 2020 to 2025
$1.8M
Targeting autophagy to increase the sensitivity of LKB1-deficient lung tumors to angiogenesis inhibitorR21CA263136 · NCI · RUTGERS BIOMEDICAL AND HEALTH SCIENCES · PI GUO, YANXIANG · 2022 to 2023
$400k
NCI NIH HHS OT2 CA278609NCI NIH HHS R01 CA163591NCI NIH HHS R01 CA237347NCI NIH HHS R21 CA263136
6 · The paper itself

Abstract

Macroautophagy (autophagy hereafter) is an intracellular nutrient scavenging pathway induced by starvation and other stressors whereby cellular components such as organelles are captured in double-membrane vesicles (autophagosomes), whereupon their contents are degraded through fusion with lysosomes. Two main purposes of autophagy are to recycle the intracellular breakdown products to sustain metabolism and survival during starvation and to eliminate damaged or excess cellular components to suppress inflammation and maintain homeostasis. In contrast to most normal cells and tissues in the fed state, tumor cells up-regulate autophagy to promote their growth, survival, and malignancy. This tumor-cell-autonomous autophagy supports elevated metabolic demand and suppresses tumoricidal activation of the innate and adaptive immune responses. Tumor-cell-nonautonomous (e.g., host) autophagy also supports tumor growth by maintaining essential tumor nutrients in the circulation and tumor microenvironment and by suppressing an antitumor immune response. In the setting of cancer therapy, autophagy is a resistance mechanism to chemotherapy, targeted therapy, and immunotherapy. Thus, tumor and host autophagy are protumorigenic and autophagy inhibition is being examined as a novel therapeutic approach to treat cancer.

Indexed as

AutophagyNeoplasmsTumor MicroenvironmentAnimalsHumans

Identifiers

PMID38253423
PMCPMC11216174
OpenAlexW4391099131

What Socratic holds

Textmetadata
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 Socratic graph.