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Updated: Sep 10, 2025

In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice
Published on: August 23, 2019
MicroRNA-mediated autophagy regulation in thyroid cancer drug resistance
Dongye Huang1,2, Qianwen Liu1,2, Chang Liu3,2
1State Key Laboratory of Oncology in South China, Guangdong Provincial Clinical Research Center for Cancer, Sun Yat-sen University Cancer Center, Guangzhou 510060, Guangdong, China.
Abstract:
Thyroid cancer, particularly papillary thyroid cancer (PTC), represents the most prevalent endocrine malignancy. Despite advancements in therapeutic strategies, drug resistance significantly hampers clinical outcomes. Autophagy, an evolutionarily conserved cellular degradation pathway, acts paradoxically in thyroid cancer by promoting either tumor cell survival or cell death, thus influencing therapeutic resistance. Increasing evidence highlights microRNAs (miRNAs), small non-coding RNAs, as critical regulators of autophagy through precise modulation of autophagy-related genes (ATGs) and signaling pathways. miRNA-mediated autophagy can either enhance chemotherapeutic efficacy or facilitate resistance, depending on the cellular context and miRNA targets. This review summarizes recent insights into miRNA-autophagy interactions underlying drug resistance in thyroid cancer, emphasizing key miRNAs, including miR-125b, miR-144, miR-30d, and miR-9-5p. Understanding the complex regulatory networks connecting miRNAs and autophagy provides promising avenues for developing novel therapeutic strategies to overcome resistance in refractory thyroid cancer.
Insights
MicroRNAs (miRNAs) and autophagy play dual roles in thyroid cancer drug resistance. Understanding their interactions, like those involving miR-125b, offers new strategies for treating resistant thyroid cancers.
Area of Science:
- Endocrinology
- Molecular Biology
- Oncology
Background:
- Papillary thyroid cancer (PTC) is the most common endocrine malignancy.
- Drug resistance remains a major challenge in treating thyroid cancer effectively.
- Autophagy, a cellular process, has a complex role in thyroid cancer, influencing both survival and cell death.
Purpose of the Study:
- To review the intricate relationship between microRNAs (miRNAs) and autophagy in the context of thyroid cancer drug resistance.
- To highlight specific miRNAs and their impact on autophagy-related genes and pathways.
- To explore the potential of targeting miRNA-autophagy interactions for novel therapeutic strategies.
Main Methods:
- Literature review focusing on recent studies of miRNA-autophagy interactions in thyroid cancer.
- Analysis of key miRNAs (e.g., miR-125b, miR-144, miR-30d, miR-9-5p) and their targets.
- Examination of the dual role of autophagy in modulating therapeutic resistance.
Main Results:
- miRNAs critically regulate autophagy by modulating autophagy-related genes (ATGs).
- miRNA-mediated autophagy can either sensitize cancer cells to chemotherapy or promote drug resistance.
- Specific miRNAs like miR-125b, miR-144, miR-30d, and miR-9-5p are implicated in this process.
Conclusions:
- The interplay between miRNAs and autophagy is a key determinant of drug resistance in thyroid cancer.
- Targeting these regulatory networks presents a promising approach to overcome resistance in refractory thyroid cancer.
- Further research into these complex interactions could lead to innovative therapeutic interventions.
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