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Published on: October 28, 2019
α-Solanine induces ROS-mediated autophagy through activation of endoplasmic reticulum stress and inhibition of
M Hasanain1, A Bhattacharjee2, P Pandey1
1Biochemistry Division, CSIR-Central Drug Research Institute, Lucknow, India.
Abstract:
α-Solanine is a glycoalkaloid found in species of the nightshade family including potato. It was primarily reported to have toxic effects in humans. However, there is a growing body of literature demonstrating in vitro and in vivo anticancer activity of α-solanine. Most of these studies have shown activation of apoptosis as the underlying mechanism in antitumor activity of α-solanine. In this study, we report α-solanine as a potential inducer of autophagy, which may act synergistically or in parallel with apoptosis to exert its cytotoxic effect. Induction of autophagy was demonstrated by several assays including electron microscopy, immunoblotting of autophagy markers and immunofluorescence for LC3 (microtubule-associated protein 1 (MAP1) light chain-3) puncta. α-Solanine-induced autophagic flux was demonstrated by additionally enhanced--turnover of LC3-II and--accumulation of LC3-specific puncta after co-incubation of cells with either of the autophagolysosome inhibitors--chloroquine and--bafilomycin A1. We also demonstrated α-solanine-induced oxidative damage in regulating autophagy where pre-incubation of cells with reactive oxygen species (ROS) scavenger resulted in suppression of CM-H2DCFDA (5 (and 6)-chloromethyl-2',7'-dichlorodihydrofluorescein diacetate acetyl ester) fluorescence as well as decrease in LC3-II turnover. α-Solanine treatment caused an increase in the expression of endoplasmic reticulum (ER) stress proteins (BiP, activating transcription factor 6 (ATF6), X-box-binding protein 1, PERK, inositol-requiring transmembrane kinase/endonuclease 1, ATF4 and CCAAT-enhancer-binding protein (C/EBP)-homologous protein) suggesting activation of unfolded protein response pathway. Moreover, we found downregulation of phosphorylated Akt (Thr308 and Ser473), mammalian target of rapamycin (mTOR; Ser2448 and Ser2481) and 4E-BP1 (Thr37/46) by α-solanine implying suppression of the Akt/mTOR pathway. Collectively, our results signify that α-solanine induces autophagy to exert anti-proliferative activity by triggering ER stress and inhibiting Akt/mTOR signaling pathway.
Insights
α-Solanine, found in nightshade plants, shows anticancer potential by inducing autophagy, a cellular process that may work alongside apoptosis. This study reveals its role in triggering endoplasmic reticulum stress and inhibiting key signaling pathways for anti-proliferative effects.
Area of Science:
- Biochemistry
- Cell Biology
- Pharmacology
Background:
- α-Solanine, a glycoalkaloid from nightshade plants, is known for toxicity but also exhibits anticancer properties.
- Previous research linked α-solanine's antitumor effects to apoptosis induction.
- Emerging evidence suggests autophagy may also play a role in its cytotoxic mechanisms.
Purpose of the Study:
- To investigate α-solanine's role as an autophagy inducer.
- To explore the interplay between autophagy, apoptosis, and oxidative stress in α-solanine's anticancer activity.
- To elucidate the signaling pathways affected by α-solanine, including endoplasmic reticulum stress and Akt/mTOR.
Main Methods:
- Electron microscopy and immunofluorescence for autophagy markers (LC3).
- Autophagic flux assays using lysosome inhibitors (chloroquine, bafilomycin A1).
- Assessment of oxidative stress, endoplasmic reticulum stress proteins, and Akt/mTOR pathway components.
Main Results:
- α-Solanine induced autophagy, confirmed by LC3 puncta and flux assays.
- Autophagy induction was linked to oxidative damage and endoplasmic reticulum stress.
- α-Solanine suppressed the Akt/mTOR signaling pathway, indicated by reduced phosphorylation of Akt, mTOR, and 4E-BP1.
Conclusions:
- α-Solanine induces autophagy, potentially acting synergistically with apoptosis for cytotoxic effects.
- The anti-proliferative activity of α-solanine involves triggering endoplasmic reticulum stress and inhibiting the Akt/mTOR pathway.
- α-Solanine presents a potential therapeutic agent for cancer, with autophagy induction as a key mechanism.
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