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Methoxyhispolon Methyl Ether, a Hispolon Analog, Thwarts the SRC/STAT3/BCL-2 Axis to Provoke Human Triple-Negative
Chih-Pin Liao1,2, Ya-Chu Hsieh3, Chien-Hsing Lu2,4
1Division of General Surgery, Department of Surgery, Kuang Tien General Hospital, Taichung 433401, Taiwan.
Abstract:
Triple-negative breast cancer (TNBC) is the most aggressive subtype of breast cancer with few treatment options. A promising TNBC treatment approach is targeting the oncogenic signaling pathways pivotal to TNBC initiation and progression. Deregulated activation of signal transducer and activator of transcription 3 (STAT3) is fundamental to driving TNBC malignant transformation, highlighting STAT3 as a promising TNBC therapeutic target. Methoxyhispolon Methyl Ether (MHME) is an analog of Hispolon, an anti-cancer polyphenol found in the medicinal mushroom Phellinus linteus. Still, MHME's anti-cancer effects and mechanisms remain unknown. Herein, we present the first report about MHME's anti-TNBC effect and its action mechanism. We first revealed that MHME is proapoptotic and cytotoxic against human TNBC cell lines HS578T, MDA-MB-231, and MDA-MB-463 and displayed a more potent cytotoxicity than Hispolon's. Mechanistically, MHME suppressed both constitutive and interleukin 6 (IL-6)-induced activation of STAT3 represented by the extent of tyrosine 705-phosphorylated STAT3 (p-STAT3). Notably, MHME-evoked apoptosis and clonogenicity impairment were abrogated in TNBC cells overexpressing a dominant-active mutant of STAT3 (STAT3-C); supporting the blockade of STAT3 activation is an integral mechanism of MHME's cytotoxic action on TNBC cells. Moreover, MHME downregulated BCL-2 in a STAT3-dependent manner, and TNBC cells overexpressing BCL-2 were refractory to MHME-induced apoptosis, indicating that BCL-2 downregulation is responsible for MHME's proapoptotic effect on TNBC cells. Finally, MHME suppressed SRC activation, while v-src overexpression rescued p-STAT3 levels and downregulated apoptosis in MHME-treated TNBC cells. Collectively, we conclude that MHME provokes TNBC cell apoptosis through the blockade of the SRC/STAT3/BCL-2 pro-survival axis. Our findings suggest the potential of applying MHME as a TNBC chemotherapy agent.
Insights
Methoxyhispolon Methyl Ether (MHME) effectively targets triple-negative breast cancer (TNBC) by inhibiting the SRC/STAT3/BCL-2 pathway. This novel compound shows potent anti-cancer effects, offering a promising new chemotherapy agent for TNBC treatment.
Area of Science:
- Oncology
- Molecular Biology
- Pharmacology
Background:
- Triple-negative breast cancer (TNBC) is an aggressive subtype with limited therapeutic options.
- Targeting oncogenic signaling pathways, particularly signal transducer and activator of transcription 3 (STAT3), is a key strategy for TNBC treatment.
- Methoxyhispolon Methyl Ether (MHME), a Hispolon analog, has unknown anti-cancer properties.
Purpose of the Study:
- To investigate the anti-TNBC effects of MHME.
- To elucidate the underlying molecular mechanisms of MHME's action against TNBC.
Main Methods:
- Assessed MHME's cytotoxicity and apoptosis-inducing effects on human TNBC cell lines (HS578T, MDA-MB-231, MDA-MB-463).
- Investigated MHME's impact on STAT3 activation (p-STAT3), BCL-2 expression, and SRC activation.
- Utilized dominant-active STAT3 mutant and v-src overexpression to confirm the mechanism of action.
Main Results:
- MHME exhibited potent proapoptotic and cytotoxic effects against TNBC cell lines, surpassing Hispolon.
- MHME suppressed both constitutive and IL-6-induced STAT3 activation in a STAT3-dependent manner.
- MHME downregulated BCL-2 expression and inhibited SRC activation, leading to apoptosis induction.
Conclusions:
- MHME effectively induces apoptosis in TNBC cells by blocking the SRC/STAT3/BCL-2 pro-survival axis.
- MHME demonstrates potential as a novel chemotherapy agent for treating triple-negative breast cancer.
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