Related Experiment Video
Updated: Apr 21, 2026

Performing Data Mining And Integrative Analysis Of Biomarker in Breast Cancer Using Multiple Publicly Accessible Databases
Published on: May 17, 2019
The Quartet of Core Oncogenic Drivers in Neuroendocrine Prostate Cancer: Multi-Omics Dataset Integration to Forge a
Youzhi Wang1, Ning Wu2, Junbo Li3
1Department of Urology, Peking University Third Hospital, Beijing, 100191, China.
Abstract:
Prostate cancer (PC) is the most common cancer among American men and the second leading cause of cancer-related deaths. For advanced or metastatic PC, anti-androgen therapies, including androgen deprivation therapy (ADT), are considered standard treatment options. However, these therapies often result in the development of castration-resistant prostate cancer (CRPC) or neuroendocrine prostate cancer (NEPC), both of which present significant treatment challenge. The molecular mechanisms driving the progression from androgen - sensitive PC to castration-resistant and neuroendocrine phenotypes are still being actively investigated. This review aims to comprehensively evaluate the cellular and molecular mechanisms underlying the development of NEPC. Specifically, it will focus on the roles of cancer stem cells (CSCs), epithelial - mesenchymal transition (EMT), and autophagy in the pathogenesis and progression of NEPC. Furthermore, the review will explore the potential of targeting these processes for therapeutic intervention in advanced P. This review will integrate current findings from clinical trials, pre-clinical models, and molecular research to clarify the promising approaches for improving treatment outcomes for patients with advanced PC.
Insights
Neuroendocrine prostate cancer (NEPC) arises from advanced prostate cancer (PC) despite anti-androgen therapies. This review explores cancer stem cells, EMT, and autophagy roles in NEPC development and potential therapeutic targets.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Research
Background:
- Prostate cancer (PC) is a leading cause of cancer death in men.
- Advanced PC treatments like androgen deprivation therapy (ADT) can lead to castration-resistant (CRPC) and neuroendocrine (NEPC) forms.
- The mechanisms driving PC progression to NEPC remain under investigation.
Purpose of the Study:
- To comprehensively review cellular and molecular mechanisms of NEPC development.
- To focus on the roles of cancer stem cells (CSCs), epithelial-mesenchymal transition (EMT), and autophagy in NEPC pathogenesis.
- To explore therapeutic strategies targeting these pathways for advanced PC.
Main Methods:
- Literature review integrating clinical trials, pre-clinical models, and molecular research.
- Analysis of cellular mechanisms including CSCs, EMT, and autophagy.
- Evaluation of potential therapeutic interventions targeting identified pathways.
Main Results:
- NEPC development is linked to complex molecular changes following ADT.
- CSCs, EMT, and autophagy are implicated as key drivers in NEPC progression.
- Targeting these mechanisms shows promise for overcoming treatment resistance.
Conclusions:
- Understanding NEPC pathogenesis is crucial for improving outcomes in advanced prostate cancer.
- Targeting CSCs, EMT, and autophagy offers potential therapeutic avenues.
- Further research integrating clinical and molecular data is needed to refine treatment strategies.
More Related Videos
12:13Sequencing Small Non-coding RNA from Formalin-fixed Tissues and Serum-derived Exosomes from Castration-resistant Prostate Cancer Patients
Published on: November 19, 2019
07:34Author Spotlight: Advancing Prostate Cancer Research Through Improved Tissue Sampling and Biobanking
Published on: November 17, 2023
Related Concept Videos
Mouse Models of Cancer Study
The development of transgenic, knockout, and knock-in mice has led to an exponential increase in their use as model organisms in research,...
Mouse Models of Cancer Study
Tumor Progression
Colon cancer is one of the best-documented examples of tumor progression. Early mutation in the APC gene in colon cells causes a small growth on the colon wall called a polyp. With time, this polyp grows into a benign, pre-cancerous tumor. Further...
Tumor Progression
Proteomics
Proteomics is the study of proteomes' function. It involves the large-scale systematic study of the proteome to denote the protein complement expressed by a genome. Scientist Mark Wilkins coined the term...
Cancer-Critical Genes I: Proto-oncogenes
When the function of certain critical genes, especially those involved in cell cycle regulation and cell growth signaling cascades, gets disrupted, it upsets the cell cycle progression. Such cells with unchecked cell cycles start proliferating uncontrollably and eventually develop into tumors.
Such genes that act...