Evidence map›Paper›PMID 35884592›Full record

ReviewCancers2022

Autophagy: A Key Player in Pancreatic Cancer Progression and a Potential Drug Target.

Josef Gillson, Yomna S Abd El-Aziz, Lionel Y W Leck, Patric J Jansson, Nick Pavlakis, Jaswinder S Samra, Anubhav Mittal, Sumit Sahni

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
5.1field-weighted citation impact, top 4% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

  1. Pooled it
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  7. Article
  8. Autophagy: The convergence point of aging and cancer.Biochemistry and biophysics reports · 2025
    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

8 authors at 1 institution in 2 countries.

Josef GillsonFaculty of Medicine and Health, University of Sydney, Camperdown, Sydney, NSW 2050, Australia.ORCID 0000-0002-0884-3972
Yomna S Abd El-AzizFaculty of Medicine and Health, University of Sydney, Camperdown, Sydney, NSW 2050, Australia.
Lionel Y W LeckFaculty of Medicine and Health, University of Sydney, Camperdown, Sydney, NSW 2050, Australia.
Patric J JanssonFaculty of Medicine and Health, University of Sydney, Camperdown, Sydney, NSW 2050, Australia.ORCID 0000-0002-9322-653X
Nick PavlakisFaculty of Medicine and Health, University of Sydney, Camperdown, Sydney, NSW 2050, Australia.ORCID 0000-0002-1738-0316
Jaswinder S SamraFaculty of Medicine and Health, University of Sydney, Camperdown, Sydney, NSW 2050, Australia.
Anubhav MittalFaculty of Medicine and Health, University of Sydney, Camperdown, Sydney, NSW 2050, Australia.
Sumit SahniFaculty of Medicine and Health, University of Sydney, Camperdown, Sydney, NSW 2050, Australia.ORCID 0000-0002-2900-8845
The University of Sydney · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pancreatic cancer is known to have the lowest survival outcomes among all major cancers, and unfortunately, this has only been marginally improved over last four decades. The innate characteristics of pancreatic cancer include an aggressive and fast-growing nature from powerful driver mutations, a highly defensive tumor microenvironment and the upregulation of advantageous survival pathways such as autophagy. Autophagy involves targeted degradation of proteins and organelles to provide a secondary source of cellular supplies to maintain cell growth. Elevated autophagic activity in pancreatic cancer is recognized as a major survival pathway as it provides a plethora of support for tumors by supplying vital resources, maintaining tumour survival under the stressful microenvironment and promoting other pathways involved in tumour progression and metastasis. The combination of these features is unique to pancreatic cancer and present significant resistance to chemotherapeutic strategies, thus, indicating a need for further investigation into therapies targeting this crucial pathway. This review will outline the autophagy pathway and its regulation, in addition to the genetic landscape and tumor microenvironment that contribute to pancreatic cancer severity. Moreover, this review will also discuss the mechanisms of novel therapeutic strategies that inhibit autophagy and how they could be used to suppress tumor progression.

Indexed as

autophagyautophagy inhibitorspancreatic ductal adenocarcinomastresstumor microenvironment

Identifiers

PMID35884592
PMCPMC9315706
OpenAlexW4286005638

What Socratic 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 Socratic graph.