| Literature DB >> 33535613 |
Chie Kudo-Saito1, Yukinori Ozaki1, Hiroshi Imazeki1, Hideyuki Hayashi1, Jun Masuda1, Hiroki Ozawa1, Yamato Ogiwara1.
Abstract
Residual metastasis is a major cause of cancer-associated death. Recent advances in understanding the molecular basis of the epithelial-mesenchymal transition (EMT) and the related cancer stem cells (CSCs) have revealed the landscapes of cancer metastasis and are promising contributions to clinical treatments. However, this rarely leads to practical advances in the management of cancer in clinical settings, and thus cancer metastasis is still a threat to patients. The reason for this may be the heterogeneity and complexity caused by the evolutional transformation of tumor cells through interactions with the host environment, which is composed of numerous components, including stromal cells, vascular cells, and immune cells. The reciprocal evolution further raises the possibility of successful tumor escape, resulting in a fatal prognosis for patients. To disrupt the vicious spiral of tumor-immunity aggravation, it is important to understand the entire metastatic process and the practical implementations. Here, we provide an overview of the molecular and cellular links between tumors' biological properties and host immunity, mainly focusing on EMT and CSCs, and we also highlight therapeutic agents targeting the oncoimmune determinants driving cancer metastasis toward better practical use in the treatment of cancer patients.Entities:
Keywords: EMT; cancer stem; immune checkpoint; immune dysfunction; immune exhaustion; immunity; immunosuppression; immunotherapy; metastasis; polyploidization
Year: 2021 PMID: 33535613 DOI: 10.3390/cancers13030554
Source DB: PubMed Journal: Cancers (Basel) ISSN: 2072-6694 Impact factor: 6.639