Gabel Austin M, Crosse Edie I, Belleville Andrea E, Hogg Simon J, McKellar Siegen A, Abdel-Wahab Omar, Thomas James D, Bradley Robert K
Computational Biology Program, Public Health Sciences Division, Fred Hutchinson Cancer Center, Seattle, Washington, United States of America.
Basic Sciences Division, Fred Hutchinson Cancer Center, Seattle, Washington, United States of America.
PLoS One. 2025 Apr 30;20(4):e0321148. doi: 10.1371/journal.pone.0321148. eCollection 2025.
Exploiting the immune system to eradicate cancer cells is an area of intense clinical study. However, the mechanisms that shape the tumor-immune microenvironment are incompletely understood. Here, we identify Muscleblind-like (MBNL) proteins as novel modulators of the tumor-immune microenvironment across diverse cancers. We demonstrate that loss of tumor MBNL expression results in an attenuated response to interferon gamma and reduced tumor antigen presentation in melanoma, breast cancer, and colorectal cancer cells. Parallel experiments in a syngeneic mouse melanoma model revealed that MBNL loss reduces tumor cell killing by CD8 + T cells in vitro and facilitates tumor escape from cytotoxic CD8 + T cell infiltration in vivo. Finally, we extended these studies to 29 human cancer types to find that MBNL expression levels are strongly associated with gene expression signatures of T cell tumor infiltration. These insights suggest that MBNL proteins play important roles in shaping the immune landscape across diverse malignancies.
利用免疫系统根除癌细胞是一个正在深入进行临床研究的领域。然而,塑造肿瘤免疫微环境的机制尚未完全明确。在此,我们确定肌肉盲样(MBNL)蛋白是多种癌症中肿瘤免疫微环境的新型调节因子。我们证明,肿瘤中MBNL表达缺失会导致黑色素瘤、乳腺癌和结肠癌细胞对干扰素γ的反应减弱以及肿瘤抗原呈递减少。在同基因小鼠黑色素瘤模型中进行的平行实验表明,MBNL缺失在体外会减少CD8 + T细胞对肿瘤细胞的杀伤,并在体内促进肿瘤逃避细胞毒性CD8 + T细胞的浸润。最后,我们将这些研究扩展到29种人类癌症类型,发现MBNL表达水平与T细胞肿瘤浸润的基因表达特征密切相关。这些见解表明,MBNL蛋白在塑造多种恶性肿瘤的免疫格局中发挥着重要作用。