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Targeting oncogenic Myc as a strategy for cancer treatment
Hui Chen1,2, Hudan Liu1,2, Guoliang Qing1,2
11Zhongnan Hospital of Wuhan University, Wuhan, People's Republic of China.
Abstract:
The MYC family oncogene is deregulated in >50% of human cancers, and this deregulation is frequently associated with poor prognosis and unfavorable patient survival. Myc has a central role in almost every aspect of the oncogenic process, orchestrating proliferation, apoptosis, differentiation, and metabolism. Although Myc inhibition would be a powerful approach for the treatment of many types of cancers, direct targeting of Myc has been a challenge for decades owing to its "undruggable" protein structure. Hence, alternatives to Myc blockade have been widely explored to achieve desirable anti-tumor effects, including Myc/Max complex disruption, MYC transcription and/or translation inhibition, and Myc destabilization as well as the synthetic lethality associated with Myc overexpression. In this review, we summarize the latest advances in targeting oncogenic Myc, particularly for cancer therapeutic purposes.
Insights
The MYC oncogene drives over half of human cancers. This review explores novel therapeutic strategies to target MYC, offering new hope for effective cancer treatment.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Genetics
Background:
- The MYC oncogene is frequently deregulated in human cancers, correlating with poor prognosis.
- MYC plays a critical role in regulating cell proliferation, apoptosis, differentiation, and metabolism.
- Directly inhibiting MYC is challenging due to its 'undruggable' protein structure.
Purpose of the Study:
- To review recent advancements in targeting oncogenic MYC for cancer therapy.
- To explore alternative strategies for MYC inhibition beyond direct blockade.
Main Methods:
- Literature review of studies on MYC targeting strategies.
- Analysis of approaches including Myc/Max complex disruption, MYC transcription/translation inhibition, MYC destabilization, and synthetic lethality.
Main Results:
- Several alternative strategies show promise in achieving anti-tumor effects.
- These include targeting MYC interactions, expression, and dependencies.
Conclusions:
- Targeting MYC remains a critical goal in cancer therapy.
- Emerging strategies offer viable alternatives to direct MYC inhibition, advancing cancer treatment possibilities.
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