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MicroRNA-203a-3p as a Modulator of Doxorubicin Resistance in Hepatocellular Carcinoma: Molecular and Metabolic Insights

Hepatocellular carcinoma (HCC) continues to be a significant global health concern, ranking third in mortality rates among all cancer types. Despite therapeutic advancements, doxorubicin (DOX) remains a cornerstone chemotherapeutic agent in the treatment of HCC. However, its efficacy is often limite...

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Main Author: Abdelaal, Noha Mohamed
Format: Thesis
Published: AUC Knowledge Fountain 2026
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access_status_str Open Access
author Abdelaal, Noha Mohamed
author_browse Abdelaal, Noha Mohamed
author_facet Abdelaal, Noha Mohamed
author_sort Abdelaal, Noha Mohamed
collection Thesis
description Hepatocellular carcinoma (HCC) continues to be a significant global health concern, ranking third in mortality rates among all cancer types. Despite therapeutic advancements, doxorubicin (DOX) remains a cornerstone chemotherapeutic agent in the treatment of HCC. However, its efficacy is often limited by the development of drug resistance. Increased cellular capacity to repair DNA damage is a key molecular mechanism underlying DOX resistance. MicroRNAs (miRNAs) are a family of small, non-protein-coding RNA molecules that regulate gene expression post-transcriptionally. They have emerged as critical regulators of tumorigenesis and are considered promising biomarkers and therapeutic targets. Among them, miR-203a-3p has been implicated in modulating chemoresistance in various cancer types, though its role in HCC remains unclear. In this study, we employed a comprehensive approach to investigate the functional role of miR-203a-3p in response to DOX treatment in HCC. To elucidate the underlying mechanisms, we combined cytotoxicity assays, gene expression analysis, apoptosis assays, and metabolic profiling, using HepG2 and Huh7 cells, which differ in p53 status. Our findings offer new insights into the role of miR-203a-3p in the context of HCC chemoresistance, with potential implications for therapeutic interventions. Understanding the molecular and metabolic underpinnings of miR-203a3p function may inform the development of more effective miRNA-based combination therapies to overcome chemoresistance and improve treatment outcomes.
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institution American University in Cairo (Egypt)
last_indexed 2026-06-10T12:35:59.828Z
license_str Not specified — see source repository
provenance_str_mv Harvested via OAI-PMH from AUC Knowledge Fountain — bepress
publishDate 2026
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spelling oai:fount.aucegypt.edu:etds-3673 MicroRNA-203a-3p as a Modulator of Doxorubicin Resistance in Hepatocellular Carcinoma: Molecular and Metabolic Insights Abdelaal, Noha Mohamed Hepatocellular carcinoma (HCC) continues to be a significant global health concern, ranking third in mortality rates among all cancer types. Despite therapeutic advancements, doxorubicin (DOX) remains a cornerstone chemotherapeutic agent in the treatment of HCC. However, its efficacy is often limited by the development of drug resistance. Increased cellular capacity to repair DNA damage is a key molecular mechanism underlying DOX resistance. MicroRNAs (miRNAs) are a family of small, non-protein-coding RNA molecules that regulate gene expression post-transcriptionally. They have emerged as critical regulators of tumorigenesis and are considered promising biomarkers and therapeutic targets. Among them, miR-203a-3p has been implicated in modulating chemoresistance in various cancer types, though its role in HCC remains unclear. In this study, we employed a comprehensive approach to investigate the functional role of miR-203a-3p in response to DOX treatment in HCC. To elucidate the underlying mechanisms, we combined cytotoxicity assays, gene expression analysis, apoptosis assays, and metabolic profiling, using HepG2 and Huh7 cells, which differ in p53 status. Our findings offer new insights into the role of miR-203a-3p in the context of HCC chemoresistance, with potential implications for therapeutic interventions. Understanding the molecular and metabolic underpinnings of miR-203a3p function may inform the development of more effective miRNA-based combination therapies to overcome chemoresistance and improve treatment outcomes. 2026-01-31T08:00:00Z thesis application/pdf https://fount.aucegypt.edu/etds/2617 https://fount.aucegypt.edu/context/etds/article/3673/viewcontent/Noha_Mohamed_Abdelaal_Thesis.pdf Theses and Dissertations AUC Knowledge Fountain Hepatocellular Carcinoma; Doxorubicin Resistance; miR-203a-3p; p53 Signaling; TAp63 Signaling; Apoptosis; Metabolic Rewiring Life Sciences Medicine and Health Sciences
spellingShingle Hepatocellular Carcinoma; Doxorubicin Resistance; miR-203a-3p; p53 Signaling; TAp63 Signaling; Apoptosis; Metabolic Rewiring
Life Sciences
Medicine and Health Sciences
Abdelaal, Noha Mohamed
MicroRNA-203a-3p as a Modulator of Doxorubicin Resistance in Hepatocellular Carcinoma: Molecular and Metabolic Insights
title MicroRNA-203a-3p as a Modulator of Doxorubicin Resistance in Hepatocellular Carcinoma: Molecular and Metabolic Insights
title_full MicroRNA-203a-3p as a Modulator of Doxorubicin Resistance in Hepatocellular Carcinoma: Molecular and Metabolic Insights
title_fullStr MicroRNA-203a-3p as a Modulator of Doxorubicin Resistance in Hepatocellular Carcinoma: Molecular and Metabolic Insights
title_full_unstemmed MicroRNA-203a-3p as a Modulator of Doxorubicin Resistance in Hepatocellular Carcinoma: Molecular and Metabolic Insights
title_short MicroRNA-203a-3p as a Modulator of Doxorubicin Resistance in Hepatocellular Carcinoma: Molecular and Metabolic Insights
title_sort microrna 203a 3p as a modulator of doxorubicin resistance in hepatocellular carcinoma molecular and metabolic insights
topic Hepatocellular Carcinoma; Doxorubicin Resistance; miR-203a-3p; p53 Signaling; TAp63 Signaling; Apoptosis; Metabolic Rewiring
Life Sciences
Medicine and Health Sciences
url https://fount.aucegypt.edu/etds/2617
https://fount.aucegypt.edu/context/etds/article/3673/viewcontent/Noha_Mohamed_Abdelaal_Thesis.pdf
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