TY - JOUR
T1 - Bridging the gap
T2 - advancing cancer cell culture to reveal key metabolic targets
AU - Kes, Marjolein M G
AU - Berkers, Celia R
AU - Drost, Jarno
N1 - Copyright © 2024 Kes, Berkers and Drost.
PY - 2024
Y1 - 2024
N2 - Metabolic rewiring is a defining characteristic of cancer cells, driving their ability to proliferate. Leveraging these metabolic vulnerabilities for therapeutic purposes has a long and impactful history, with the advent of antimetabolites marking a significant breakthrough in cancer treatment. Despite this, only a few in vitro metabolic discoveries have been successfully translated into effective clinical therapies. This limited translatability is partially due to the use of simplistic in vitro models that do not accurately reflect the tumor microenvironment. This Review examines the effects of current cell culture practices on cancer cell metabolism and highlights recent advancements in establishing more physiologically relevant in vitro culture conditions and technologies, such as organoids. Applying these improvements may bridge the gap between in vitro and in vivo findings, facilitating the development of innovative metabolic therapies for cancer.
AB - Metabolic rewiring is a defining characteristic of cancer cells, driving their ability to proliferate. Leveraging these metabolic vulnerabilities for therapeutic purposes has a long and impactful history, with the advent of antimetabolites marking a significant breakthrough in cancer treatment. Despite this, only a few in vitro metabolic discoveries have been successfully translated into effective clinical therapies. This limited translatability is partially due to the use of simplistic in vitro models that do not accurately reflect the tumor microenvironment. This Review examines the effects of current cell culture practices on cancer cell metabolism and highlights recent advancements in establishing more physiologically relevant in vitro culture conditions and technologies, such as organoids. Applying these improvements may bridge the gap between in vitro and in vivo findings, facilitating the development of innovative metabolic therapies for cancer.
UR - http://www.ncbi.nlm.nih.gov/pubmed/39355125
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=PMC11442172
UR - https://www.mendeley.com/catalogue/948d7fae-5b5d-3355-b68c-44728d5cf0ac/
U2 - 10.3389/fonc.2024.1480613
DO - 10.3389/fonc.2024.1480613
M3 - Review article
C2 - 39355125
SN - 2234-943X
VL - 14
SP - 1480613
JO - Frontiers in Oncology
JF - Frontiers in Oncology
ER -