Analysis of neuroglia and immune cells in the tumor microenvironment of breast cancer brain metastasis

被引:6
作者
Mo, Haixin [1 ]
Zhang, Xin [1 ,2 ,3 ]
Ren, Liangliang [1 ]
机构
[1] Jiangmen Cent Hosp, Jiangmen Engn Technol Res Ctr Clin Biobank & Trans, Clin Expt Ctr, Jiangmen, Peoples R China
[2] Guangdong Med Univ, Dongguan Key Lab Med Bioact Mol Dev & Translat Res, Guangdong Prov Key Lab Med Mol Diagnost, Dongguan, Peoples R China
[3] Guangdong Med Univ, Collaborat Innovat Ctr Antitumor Act Subst Res & D, Zhanjiang, Guangdong, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Breast cancer; brain metastasis; tumor microenvironment; neuroglia; immune cells; MACROPHAGES PROMOTE; T-CELLS; MICROGLIA; ASTROCYTES; GROWTH; TISSUE; GLIOBLASTOMA; POLARIZATION; COLONIZATION; PROGRESSION;
D O I
10.1080/15384047.2024.2398285
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Breast cancer stands as the most prevalent cancer diagnosed worldwide, often leading to brain metastasis, a challenging complication characterized by high mortality rates and a grim prognosis. Understanding the intricate mechanisms governing breast cancer brain metastasis (BCBM) remains an ongoing challenge. The unique microenvironment in the brain fosters an ideal setting for the colonization of breast cancer cells. The tumor microenvironment (TME) in brain metastases plays a pivotal role in the initiation and progression of BCBM, shaping the landscape for targeted therapeutic interventions. Current research primarily concentrates on unraveling the complexities of the TME in BCBM, with a particular emphasis on neuroglia and immune cells, such as microglia, monocyte-derived macrophages (MDMs), astrocytes and T cells. This comprehensive review delves deeply into these elements within the TME of BCBM, shedding light on their interplay, mechanisms, and potential as therapeutic targets to combat BCBM.
引用
收藏
页数:12
相关论文
共 94 条
[1]   Colony-stimulating factor-1 blockade by antisense oligonucleotides and small interfering RNAs suppresses growth of human mammary tumor xenografts in mice [J].
Aharinejad, S ;
Paulus, P ;
Sioud, M ;
Hofmann, M ;
Zins, K ;
Schäfer, R ;
Stanley, ER ;
Abraham, D .
CANCER RESEARCH, 2004, 64 (15) :5378-5384
[2]   Focused Ultrasound Delivers Targeted Immune Cells to Metastatic Brain Tumors [J].
Alkins, Ryan ;
Burgess, Alison ;
Ganguly, Milan ;
Francia, Giulio ;
Kerbel, Robert ;
Wels, Winfried S. ;
Hynynen, Kullervo .
CANCER RESEARCH, 2013, 73 (06) :1892-1899
[3]   Transcriptomic Profiling Identifies CD8+ T Cells in the Brain of Aged and Alzheimer?s Disease Transgenic Mice as Tissue-Resident Memory T Cells [J].
Altendorfer, Barbara ;
Unger, Michael Stefan ;
Poupardin, Rodolphe ;
Hoog, Anna ;
Asslaber, Daniela ;
Gratz, Iris Karina ;
Mrowetz, Heike ;
Benedetti, Ariane ;
Bessa de Sousa, Diana Marisa ;
Greil, Richard ;
Egle, Alexander ;
Gate, David ;
Wyss-Coray, Tony ;
Aigner, Ludwig .
JOURNAL OF IMMUNOLOGY, 2022, 209 (07) :1272-1285
[4]   Anti-inflammatory Microglia/Macrophages As a Potential Therapeutic Target in Brain Metastasis [J].
Andreou, Kleopatra E. ;
Soto, Manuel Sarmiento ;
Allen, Danny ;
Economopoulos, Vasiliki ;
de Bernardi, Axel ;
Larkin, James R. ;
Sibson, Nicola R. .
FRONTIERS IN ONCOLOGY, 2017, 7
[5]   Autocrine GMCSF Signaling Contributes to Growth of HER2+ Breast Leptomeningeal Carcinomatosis [J].
Ansari, Khairul, I ;
Bhan, Arunoday ;
Saotome, Mika ;
Tyagi, Antariksh ;
De Kumar, Bony ;
Chen, Clara ;
Takaku, Motoki ;
Jandial, Rahul .
CANCER RESEARCH, 2021, 81 (18) :4723-4735
[6]   Characterization of the inflammatory response to solid cancer metastases in the human brain [J].
Berghoff, Anna Sophie ;
Lassmann, Hans ;
Preusser, Matthias ;
Hoeftberger, Romana .
CLINICAL & EXPERIMENTAL METASTASIS, 2013, 30 (01) :69-81
[7]   PI3K: A master regulator of brain metastasis-promoting macrophages/microglia [J].
Blazquez, Raquel ;
Wlochowitz, Darius ;
Wolff, Alexander ;
Seitz, Stefanie ;
Wachter, Astrid ;
Perera-Bel, Julia ;
Bleckmann, Annalen ;
Beissbarth, Tim ;
Salinas, Gabriela ;
Riemenschneider, Markus J. ;
Proescholdt, Martin ;
Evert, Matthias ;
Utpatel, Kirsten ;
Siam, Laila ;
Schatlo, Bawarjan ;
Balkenhol, Marko ;
Stadelmann, Christine ;
Schildhaus, Hans-Ulrich ;
Korf, Ulrike ;
Reinz, Eileen ;
Wiemann, Stefan ;
Vollmer, Elena ;
Schulz, Mathias ;
Ritter, Uwe ;
Hanisch, Uwe K. ;
Pukrop, Tobias .
GLIA, 2018, 66 (11) :2438-2455
[8]   Regression of Glioblastoma after Chimeric Antigen Receptor T-Cell Therapy [J].
Brown, Christine E. ;
Alizadeh, Darya ;
Starr, Renate ;
Weng, Lihong ;
Wagner, Jamie R. ;
Naranjo, Araceli ;
Ostberg, Julie R. ;
Blanchard, M. Suzette ;
Kilpatrick, Julie ;
Simpson, Jennifer ;
Kurien, Anita ;
Priceman, Saul J. ;
Wang, Xiuli ;
Harshbarger, Todd L. ;
D'Apuzzo, Massimo ;
Ressler, Julie A. ;
Jensen, Michael C. ;
Barish, Michael E. ;
Chen, Mike ;
Portnow, Jana ;
Forman, Stephen J. ;
Badie, Behnam .
NEW ENGLAND JOURNAL OF MEDICINE, 2016, 375 (26) :2561-2569
[9]   Changing profiles of cancer burden worldwide and in China: a secondary analysis of the global cancer statistics 2020 [J].
Cao, Wei ;
Chen, Hong-Da ;
Yu, Yi-Wen ;
Li, Ni ;
Chen, Wan-Qing .
CHINESE MEDICAL JOURNAL, 2021, 134 (07) :783-791
[10]   Carcinoma-astrocyte gap junctions promote brain metastasis by cGAMP transfer [J].
Chen, Qing ;
Boire, Adrienne ;
Jin, Xin ;
Valiente, Manuel ;
Er, Ekrem Emrah ;
Lopez-Soto, Alejandro ;
Jacob, Leni S. ;
Patwa, Ruzeen ;
Shah, Hardik ;
Xu, Ke ;
Cross, Justin R. ;
Massague, Joan .
NATURE, 2016, 533 (7604) :493-+