» Articles » PMID: 32391363

Molecular Insights Into Therapeutic Potential of Autophagy Modulation by Natural Products for Cancer Stem Cells

Overview
Specialty Cell Biology
Date 2020 May 12
PMID 32391363
Citations 33
Authors
Affiliations
Soon will be listed here.
Abstract

Autophagy, a cellular self-digestion process that is activated in response to stress, has a functional role in tumor formation and progression. Cancer stem cells (CSCs) accounting for a minor proportion of total cancer cells-have distinct self-renewal and differentiation abilities and promote metastasis. Researchers have shown that a numeral number of natural products using traditional experimental methods have been revealed to target CSCs. However, the specific role of autophagy with respect to CSCs and tumorigenesis using natural products are still unknown. Currently, CSCs are considered to be one of the causative reasons underlying the failure of anticancer treatment as a result of tumor recurrence, metastasis, and chemo- or radio-resistance. Autophagy may play a dual role in CSC-related resistance to anticancer treatment; it is responsible for cell fate determination and the targeted degradation of transcription factors via growth arrest. It has been established that autophagy promotes drug resistance, dormancy, and stemness and maintenance of CSCs. Surprisingly, numerous studies have also suggested that autophagy can facilitate the loss of stemness in CSCs. Here, we review current progress in research related to the multifaceted connections between autophagy modulation and CSCs control using natural products. Overall, we emphasize the importance of understanding the role of autophagy in the maintenance of different CSCs and implications of this connection for the development of new strategies for cancer treatment targeting natural products.

Citing Articles

Autophagy Induction by Mangiferin Protects Auditory Hair Cells from Ototoxicity.

Lim G, Cho G, Jang C Mol Neurobiol. 2025; .

PMID: 39954163 DOI: 10.1007/s12035-025-04751-6.


Betaine inhibits the stem cell-like properties of hepatocellular carcinoma by activating autophagy via SAM/mA/YTHDF1-mediated enhancement on ATG3 stability.

Wang C, Li M, Huang W, Huang S, Wusiman M, Liu Z Theranostics. 2025; 15(5):1949-1965.

PMID: 39897540 PMC: 11780527. DOI: 10.7150/thno.102682.


Drug Target to Alleviate Mitochondrial Dysfunctions in Alzheimer's Disease: Recent Advances and Therapeutic Implications.

Rahman M, Rahman M, Rhim H, Kim B Curr Neuropharmacol. 2024; 22(12):1942-1959.

PMID: 39234772 PMC: 11333791. DOI: 10.2174/1570159X22666240426091311.


Total Synthesis of Lipopeptide Bacilotetrin C: Discovery of Potent Anticancer Congeners Promoting Autophagy.

Shankar Auddy S, Gupta S, Mandi S, Sharma H, Sinha S, Goswami R ACS Med Chem Lett. 2024; 15(8):1340-1350.

PMID: 39140062 PMC: 11318098. DOI: 10.1021/acsmedchemlett.4c00237.


Autophagy as a Therapeutic Target in Breast Tumors: The Cancer stem cell perspective.

Raza S, Siddiqui J, Srivastava A, Chattopadhyay N, Sinha R, Chakravarti B Autophagy Rep. 2024; 3(1).

PMID: 39006309 PMC: 7616179. DOI: 10.1080/27694127.2024.2358648.


References
1.
Park M, Hong J . Roles of NF-κB in Cancer and Inflammatory Diseases and Their Therapeutic Approaches. Cells. 2016; 5(2). PMC: 4931664. DOI: 10.3390/cells5020015. View

2.
Ojha R, Bhattacharyya S, Singh S . Autophagy in Cancer Stem Cells: A Potential Link Between Chemoresistance, Recurrence, and Metastasis. Biores Open Access. 2015; 4(1):97-108. PMC: 4497670. DOI: 10.1089/biores.2014.0035. View

3.
Zhang D, Zhao Q, Sun H, Yin L, Wu J, Xu J . Defective autophagy leads to the suppression of stem-like features of CD271 osteosarcoma cells. J Biomed Sci. 2016; 23(1):82. PMC: 5116184. DOI: 10.1186/s12929-016-0297-5. View

4.
Rahman M, Bishayee K, Habib K, Sadra A, Huh S . 18α-Glycyrrhetinic acid lethality for neuroblastoma cells via de-regulating the Beclin-1/Bcl-2 complex and inducing apoptosis. Biochem Pharmacol. 2016; 117:97-112. DOI: 10.1016/j.bcp.2016.08.006. View

5.
Saha S, Choi H, Kim B, Dayem A, Yang G, Kim K . KRT19 directly interacts with β-catenin/RAC1 complex to regulate NUMB-dependent NOTCH signaling pathway and breast cancer properties. Oncogene. 2016; 36(3):332-349. PMC: 5270332. DOI: 10.1038/onc.2016.221. View