Abstract |
HER2+ breast tumors have abundant immune-suppressive cells, including M2-type tumor-associated macrophages (TAMs). Although TAMs consist of the immune-stimulatory M1 type and immune-suppressive M2 type, the M1/M2-TAM ratio is reduced in immune-suppressive tumors, contributing to their immunotherapy refractoriness. M1- versus M2-TAM formation depends on differential arginine metabolism, where M1-TAMs convert arginine to nitric oxide (NO) and M2-TAMs convert arginine to polyamines (PAs). We hypothesize that such distinct arginine metabolism in M1- versus M2-TAMs is attributed to different availability of BH |
Authors |
Veani Fernando , Xunzhen Zheng , Vandana Sharma  , Osama Sweef , EunâSeok Choi , Saori Furuta
|
Journal Info |
| Life Science Alliance , vol: 7
, iss: 11
, pages: e202302339 - e202302339
|
Publication Date |
8/27/2024 |
ISSN |
2575-1077 |
Type |
article |
Open Access |
gold
|
DOI |
https://doi.org/10.26508/lsa.202302339 |
Keywords |
Reprogramming (Score: 0.48494437)
|