The Role of Macrophages in Cancer Development and Therapy.
The Role of Macrophages in Cancer Development and Therapy.
复制标题
巨噬细胞在癌症发展和治疗中的作用。
DOI:
10.3390/cancers13081946
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发表时间:
2021-04-18
期刊:
影响因子:
5.2
通讯作者:
Rygiel TP
中科院分区:
文献类型:
--
作者:
Cendrowicz E;Sas Z;Bremer E;Rygiel TP
Tumor-Associated Macrophages (TAMs) play an important role in the development of tumors, modulation of neoangiogenesis, immune suppression, and metastasis. High infiltration of macrophages in the tumor is also correlated with poor prognosis in several cancer types. Therefore, they became an attractive target for cancer immunotherapies. In this review, we describe the role of macrophages in tumorigenesis and summarize the most recent advances in the therapies targeting TAMs. Macrophages are critical mediators of tissue homeostasis and influence various aspects of immunity. Tumor-associated macrophages are one of the main cellular components of the tumor microenvironment. Depending on their activation status, macrophages can exert a dual influence on tumorigenesis by either antagonizing the cytotoxic activity of immune cells or, less frequently, by enhancing antitumor responses. In most situations, TAMs suppress T cell recruitment and function or regulate other aspects of tumor immunity. The importance of TAMs targeting in cancer therapy is derived from the strong association between the high infiltration of TAMs in the tumor tissue with poor patient prognosis. Several macrophage-targeting approaches in anticancer therapy are developed, including TAM depletion, inhibition of new TAM differentiation, or re-education of TAM activation for cancer cell phagocytosis. In this review, we will describe the role of TAMs in tumor development, including such aspects as protumorigenic inflammation, immune suppression, neoangiogenesis, and enhancement of tissue invasion and distant metastasis. Furthermore, we will discuss therapeutic approaches that aim to deplete TAMs or, on the contrary, re-educate TAMs for cancer cell phagocytosis and antitumor immunity.
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影响因子:
3.1
作者:
Brodskyn, CI;DeKrey, GK;Titus, RG
通讯作者:
Titus, RG
影响因子:
4.4
作者:
Buhtoiarov, IN;Lum, H;Rakhmilevich, AL
通讯作者:
Rakhmilevich, AL
影响因子:
10.9
作者:
Cannarile MA;Weisser M;Jacob W;Jegg AM;Ries CH;Rüttinger D
通讯作者:
Rüttinger D
影响因子:
10.9
作者:
Brempelis KJ;Cowan CM;Kreuser SA;Labadie KP;Prieskorn BM;Lieberman NAP;Ene CI;Moyes KW;Chinn H;DeGolier KR;Matsumoto LR;Daniel SK;Yokoyama JK;Davis AD;Hoglund VJ;Smythe KS;Balcaitis SD;Jensen MC;Ellenbogen RG;Campbell JS;Pierce RH;Holland EC;Pillarisetty VG;Crane CA
通讯作者:
Crane CA
影响因子:
5.4
作者:
Brana, Irene;Calles, Antonio;Calvo, Emiliano
通讯作者:
Calvo, Emiliano