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Updated: Aug 15, 2026

Analysis of SCAP N-glycosylation and Trafficking in Human Cells
Published on: November 8, 2016
The pivotal role of SCD1 in digestive cancers: Bridging lipid metabolic reprogramming and programmed cell death
Yangxi Fu1, Zheng Wang2, Lin Liu2
1Graduate School, Beijing University of Chinese Medicine, Beijing 100029, P.R. China.
Abstract:
Stearoyl‑CoA desaturase‑1 (SCD1) has emerged as a critical nexus linking lipid metabolic reprogramming to the regulation of cell death. Frequently overexpressed in digestive system malignancies ‑ including gastric, liver and colorectal cancers ‑ SCD1 represents a promising therapeutic target. This review systematically examined how SCD1, through its lipid‑modifying functions, governs three key forms of regulated cell death ‑ ferroptosis, autophagy and apoptosis ‑ thereby driving malignant progression and mediating therapy resistance in digestive cancers. Building on this mechanistic framework, the specific contributions of these regulatory pathways to tumor biology and their association with drug resistance were delineated. Current preclinical therapeutic strategies targeting SCD1 were then highlighted, encompassing both monotherapy and combination approaches with ferroptosis inducers, chemotherapeutic agents or targeted drugs. Finally, key challenges and outline future directions for drug development and clinical translation in this rapidly evolving field were discussed.
Insights
Stearoyl-CoA desaturase-1 (SCD1) links lipid metabolism and cell death in digestive cancers. Targeting SCD1 offers a promising strategy against cancer progression and therapy resistance.
Area of Science:
- Biochemistry
- Oncology
- Molecular Biology
Background:
- Stearoyl-CoA desaturase-1 (SCD1) is overexpressed in digestive cancers.
- SCD1 links lipid metabolism reprogramming to cell death regulation.
Purpose of the Study:
- To review how SCD1 governs ferroptosis, autophagy, and apoptosis in digestive cancers.
- To explore SCD1's role in malignant progression and therapy resistance.
- To discuss therapeutic strategies targeting SCD1.
Main Methods:
- Systematic review of literature.
- Analysis of SCD1's lipid-modifying functions.
- Examination of regulatory pathways in tumor biology and drug resistance.
Main Results:
- SCD1 regulates ferroptosis, autophagy, and apoptosis, driving cancer progression.
- SCD1 contributes to drug resistance in digestive malignancies.
- Preclinical strategies include SCD1 monotherapy and combinations.
Conclusions:
- SCD1 is a critical therapeutic target in digestive cancers.
- Targeting SCD1 holds potential for overcoming therapy resistance.
- Further research is needed for clinical translation.
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