Unlocking New Avenues in Multiple Myeloma Treatment: Targeting Anti-Apoptotic Genes to Enhance Drug Efficacy Público

King, Katelyn (Spring 2024)

Permanent URL: https://etd.library.emory.edu/concern/etds/nz806119c?locale=es
Published

Abstract

This study explored the role of Bcl-2 and Bcl-xL, anti-apoptotic genes known for promoting cancer cell survival, in the drug resistance of multiple myeloma by using CRISPR/Cas9 to knock them out in the KMS18 cell line. The efficacy of these knockouts was confirmed through Western blotting, and their impact on drug-induced apoptosis was assessed using Annexin-V and propidium iodide staining with flow cytometry, particularly in response to the proteasome inhibitor bortezomib. Results showed that knocking out these genes increased the susceptibility of multiple myeloma cells to apoptosis, underscoring their potential as therapeutic targets. Despite facing methodological challenges such as maintenance of cell lines and issues with co-immunoprecipitation reagents, the study offers valuable insights into overcoming drug resistance and improving treatment outcomes in multiple myeloma. Future research should investigate the combinatorial effects of these gene knockouts and develop in vivo models to further validate these findings, advancing personalized medicine in cancer treatment.

Table of Contents

INTRODUCTION

Characteristics of Cancer

Multiple Myeloma

Epidemiology Multiple Myeloma

Pathophysiology of Multiple Myeloma

Management and Treatment of Multiple Myeloma

Targeting Anti-Apoptotic Genes in Multiple Myeloma

METHODS

RESULTS

Figure 1. Western Blot Verification of Bcl-2 KO and Bcl-xL KO in KMS18 cell line.

Figure 2. First Trial of Dose-Curve Bortezomib with KMS18 Parental, Bcl-2 KO, and Bcl-xL KO cells.

Figure 3. Second Trial of Dose-Curve Bortezomib with KMS18 Parental, Bcl-2 KO, and Bcl-xL KO cells.

Figure 4. Third Trial of Dose-Curve Bortezomib with KMS18 Parental, Bcl-2 KO, and Bcl-xL KO cells.

Figure 5. Bim co-IP Actin and Bcl-xL.

DISCUSSION

REFERENCES

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