Related Experiment Video
Updated: Dec 30, 2025

Author Spotlight: A Selective Luciferase-Based Assay for Monitoring ATG4B 27 Activity in Cells
Published on: June 30, 2023
Autophagy and autophagy-related proteins in cancer
Xiaohua Li1,2,3,4, Shikun He5,6, Binyun Ma7,8
1Henan Provincial People's Hospital, Zhengzhou, 450003, China.
Abstract:
Autophagy, as a type II programmed cell death, plays crucial roles with autophagy-related (ATG) proteins in cancer. Up to now, the dual role of autophagy both in cancer progression and inhibition remains controversial, in which the numerous ATG proteins and their core complexes including ULK1/2 kinase core complex, autophagy-specific class III PI3K complex, ATG9A trafficking system, ATG12 and LC3 ubiquitin-like conjugation systems, give multiple activities of autophagy pathway and are involved in autophagy initiation, nucleation, elongation, maturation, fusion and degradation. Autophagy plays a dynamic tumor-suppressive or tumor-promoting role in different contexts and stages of cancer development. In the early tumorigenesis, autophagy, as a survival pathway and quality-control mechanism, prevents tumor initiation and suppresses cancer progression. Once the tumors progress to late stage and are established and subjected to the environmental stresses, autophagy, as a dynamic degradation and recycling system, contributes to the survival and growth of the established tumors and promotes aggressiveness of the cancers by facilitating metastasis. This indicates that regulation of autophagy can be used as effective interventional strategies for cancer therapy.
Insights
Autophagy, a cellular process involving autophagy-related proteins, has a dual role in cancer. It can suppress early tumors but promote late-stage cancer growth and metastasis.
Area of Science:
- Oncology
- Cell Biology
- Molecular Biology
Background:
- Autophagy, a programmed cell death type II, involves numerous autophagy-related (ATG) proteins and complexes.
- The precise role of autophagy in cancer progression and inhibition remains a subject of debate.
- ATG proteins orchestrate autophagy initiation, nucleation, elongation, maturation, fusion, and degradation.
Purpose of the Study:
- To elucidate the complex and context-dependent roles of autophagy in cancer development.
- To explore the mechanisms by which autophagy influences tumor suppression and promotion.
- To highlight the therapeutic potential of modulating autophagy in cancer treatment.
Main Methods:
- Review of existing literature on autophagy and cancer.
- Analysis of the functions of various ATG proteins and their complexes.
- Examination of autophagy's dynamic roles across different cancer stages.
Main Results:
- Autophagy acts as a tumor suppressor in early tumorigenesis by preventing cancer initiation.
- In established, late-stage tumors under stress, autophagy promotes survival, growth, and metastasis.
- The dual role is attributed to the complex regulation by multiple ATG proteins and pathways.
Conclusions:
- Autophagy exhibits a dynamic, stage-specific role in cancer, acting as both a suppressor and promoter.
- Understanding the intricate mechanisms of autophagy is crucial for cancer therapy.
- Targeting autophagy pathways presents a promising strategy for effective cancer interventions.
Related Concept Videos
Autophagy
An autophagic pathway consists of a series of signaling events activated in response to diverse stress and physiological conditions such as food deprivation,...
Autophagic Cell Death
Autophagy and Apoptosis
Autophagy can activate apoptosis. In normal conditions, the autophagy activating protein Beclin-1 and...
Delivery Pathways to the Lysosome
Endocytosis
In endocytosis, the cell membrane takes up macromolecules and particles from the surrounding medium. Clathrin-mediated...
mTOR Signaling and Cancer Progression
The mTOR pathway or the...
The Intrinsic Apoptotic Pathway
Adaptive Mechanisms in Cancer Cells
Some of the advantages that cancer cells have on normal cells include - enhanced ability to divide without terminally differentiating, induce new blood vessel formation,...

