OPTIMIZED METHOD FOR USING EMBRYONIC MICROENVIRONMENT TO REPROGRAM CANCER STEM CELLS

• Published in: Journal of Basic and Clinical Health Sciences Vol. 7; no. 1; p. 402
• Main Authors: Soner, Burak Cem, Oltulu, Fatih, Ozcinar, Emine, Taskiran, Aysegul, Demir, Aleyna, Acikgoz, Eda, Yuce, Zeynep, Goker, Ege Nazan Tavmergen, Oktem, Gulperi
• Format: Journal Article
• Language: English
• Published: AVES 01.01.2023
• Subjects: Analysis; Cancer; Development and progression; Diagnostic reagents industry; Embryonic stem cells; Ethylenediaminetetraacetic acid; Methods; Prostate cancer; Scientific equipment and supplies industry; Stem cells; Transplantation; Canada; United States
• ISSN: 2458-8938
• DOI: 10.30621/jbachs.1138572

Purpose: The embryonic microenvironment contains many properties that have not yet been fully explored. Our aim in this study is to report an optimized and efficient method that enables investigating the effects of the secretome of pluripotent embryonic stem cells on cancer stem cells. Material and Methods: The study is performed with a chimeric model consisted of mouse blastocysts, non cancer stem cells and human prostate cancer stem cells. Ovulation induced mice were used for blastocyst collection. DU145 prostate cancer cell line was separated into non cancer and cancer stem cells using cancer stem cell biomarker expressions by fluorescent activated cell sorting. Human prostate cancer stem cells and non cancer stem cells were microinjected into 4-day blastocyst culture in vitro by intracytoplasmic sperm injection. Results: Chimeric models provide us great convenience in basic oncological studies. In this study, using a chimeric model, we were able to study the secretome of mouse embryonic stem cells and their effect on cancer stem cells. The method is efficient and yield promising result; and could be used to study the effects on other cells as well. Conclusion: The embryonic stem cell microenvironment is suggested to have a great regenerative capacity, nowadays, the center of attraction for cancer research studies. Ethical issues restrict the human embryo studies, however, mimicking the in vivo human microenvironment with 3D cell cultures or bioprinting are now possible. Finally, optimization of new methods including 3D cell cultures with human cell lines will be a great opportunity for better understanding the reprogramming notion. Keywords: embryonic stem cells, cancer stem cells, induced pluripotent stem cells, microenvironment, secretome, intracytoplasmic sperm injection