To Detach, Migrate, Adhere, and Metastasize: CD97/ADGRE5 in Cancer

被引:19
作者
Aust, Gabriela [1 ,2 ]
Zheng, Leyu [2 ]
Quaas, Marianne [1 ]
机构
[1] Univ Leipzig, Res Labs Clin Visceral Transplantat Thorac & Vasc, Sch Med, Univ Hosp Leipzig, D-04103 Leipzig, Germany
[2] Univ Leipzig, Res Labs Clin Orthoped Traumatol & Plast Surg, Sch Med, Univ Hosp Leipzig, D-04103 Leipzig, Germany
关键词
CD97; ADGRE5; EGF-TM7; aGPCR; cancer; tumor; migration; invasion; metastasis; angiogenesis; PROTEIN-COUPLED RECEPTORS; INTESTINAL EPITHELIAL-CELLS; ADHESION GPCR FUNCTION; EGF-TM7; FAMILY; TETHERED AGONIST; BETA-CATENIN; LIGAND CD55; CD97; EXPRESSION; ACTIVATION;
D O I
10.3390/cells11091538
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Tumorigenesis is a multistep process, during which cells acquire a series of mutations that lead to unrestrained cell growth and proliferation, inhibition of cell differentiation, and evasion of cell death. Growing tumors stimulate angiogenesis, providing them with nutrients and oxygen. Ultimately, tumor cells invade the surrounding tissue and metastasize; a process responsible for about 90% of cancer-related deaths. Adhesion G protein-coupled receptors (aGPCRs) modulate the cellular processes closely related to tumor cell biology, such as adhesion and detachment, migration, polarity, and guidance. Soon after first being described, individual human aGPCRs were found to be involved in tumorigenesis. Twenty-five years ago, CD97/ADGRE5 was discovered to be induced in one of the most severe tumors, dedifferentiated anaplastic thyroid carcinoma. After decades of research, the time has come to review our knowledge of the presence and function of CD97 in cancer. In summary, CD97 is obviously induced or altered in many tumor entities; this has been shown consistently in nearly one hundred published studies. However, its high expression at circulating and tumor-infiltrating immune cells renders the systemic targeting of CD97 in tumors difficult.
引用
收藏
页数:16
相关论文
共 93 条
[11]   Physical mapping of EMR1 and CD97 in human Chromosome 19 and assignment of Cd97 to mouse Chromosome 8 suggest an ancient genomic duplication [J].
Carver, EA ;
Hamann, J ;
Olsen, AS ;
Stubbs, L .
MAMMALIAN GENOME, 1999, 10 (10) :1039-1040
[12]   CD97 stabilises the immunological synapse between dendritic cells and T cells and is targeted for degradation by the Salmonella effector SteD [J].
Cerny, Ondrej ;
Godlee, Camilla ;
Tocci, Romina ;
Cross, Nancy E. ;
Shi, Haoran ;
Williamson, James C. ;
Alix, Eric ;
Lehner, Paul J. ;
Holden, David W. .
PLOS PATHOGENS, 2021, 17 (07)
[13]   An epigenetic signature of adhesion molecules predicts poor prognosis of ovarian cancer patients [J].
Chang, Ping-Ying ;
Liao, Yu-Ping ;
Wang, Hui-Chen ;
Chen, Yu-Chih ;
Huang, Rui-Lan ;
Wang, Yu-Chi ;
Yuan, Chiou-Chung ;
Lai, Hung-Cheng .
ONCOTARGET, 2017, 8 (32) :53432-53449
[14]   Universal monitoring of minimal residual disease in acute myeloid leukemia [J].
Coustan-Smith, Elaine ;
Song, Guangchun ;
Shurtleff, Sheila ;
Yeoh, Allen Eng-Juh ;
Chng, Wee Joo ;
Chen, Siew Peng ;
Rubnitz, Jeffrey E. ;
Pui, Ching-Hon ;
Downing, James R. ;
Campana, Dario .
JCI INSIGHT, 2018, 3 (09)
[15]   New markers for minimal residual disease detection in acute lymphoblastic leukemia [J].
Coustan-Smith, Elaine ;
Song, Guangchun ;
Clark, Christopher ;
Key, Laura ;
Liu, Peixin ;
Mehrpooya, Mohammad ;
Stow, Patricia ;
Su, Xiaoping ;
Shurtleff, Sheila ;
Pui, Ching-Hon ;
Downing, James R. ;
Campana, Dario .
BLOOD, 2011, 117 (23) :6267-6276
[16]   PDZ Protein Regulation of G Protein-Coupled Receptor Trafficking and Signaling Pathways [J].
Dunn, Henry A. ;
Ferguson, Stephen S. G. .
MOLECULAR PHARMACOLOGY, 2015, 88 (04) :624-639
[17]   Enhanced expression of the complement regulatory protein CD55 predicts a poor prognosis in colorectal cancer patients [J].
Durrant, LG ;
Chapman, MA ;
Buckley, DJ ;
Spendlove, I ;
Robins, RA ;
Armitage, NC .
CANCER IMMUNOLOGY IMMUNOTHERAPY, 2003, 52 (10) :638-642
[18]   CHARACTERIZATION OF AN EARLY ACTIVATION-DEPENDENT ANTIGEN ON LYMPHOCYTES DEFINED BY THE MONOCLONAL-ANTIBODY BL-AC(F2) [J].
EICHLER, W ;
AUST, G ;
HAMANN, D .
SCANDINAVIAN JOURNAL OF IMMUNOLOGY, 1994, 39 (01) :111-115
[19]   Probability distribution of copy number alterations along the genome: an algorithm to distinguish different tumour profiles [J].
Esteves, Luisa ;
Caramelo, Francisco ;
Ribeiro, Ilda Patricia ;
Carreira, Isabel M. ;
de Melo, Joana Barbosa .
SCIENTIFIC REPORTS, 2020, 10 (01)
[20]   Analysis of the Human Tissue-specific Expression by Genome-wide Integration of Transcriptomics and Antibody-based Proteomics [J].
Fagerberg, Linn ;
Hallstrom, Bjorn M. ;
Oksvold, Per ;
Kampf, Caroline ;
Djureinovic, Dijana ;
Odeberg, Jacob ;
Habuka, Masato ;
Tahmasebpoor, Simin ;
Danielsson, Angelika ;
Edlund, Karolina ;
Asplund, Anna ;
Sjostedt, Evelina ;
Lundberg, Emma ;
Szigyarto, Cristina Al-Khalili ;
Skogs, Marie ;
Takanen, Jenny Ottosson ;
Berling, Holger ;
Tegel, Hanna ;
Mulder, Jan ;
Nilsson, Peter ;
Schwenk, Jochen M. ;
Lindskog, Cecilia ;
Danielsson, Frida ;
Mardinoglu, Adil ;
Sivertsson, Asa ;
von Feilitzen, Kalle ;
Forsberg, Mattias ;
Zwahlen, Martin ;
Olsson, IngMarie ;
Navani, Sanjay ;
Huss, Mikael ;
Nielsen, Jens ;
Ponten, Fredrik ;
Uhlen, Mathias .
MOLECULAR & CELLULAR PROTEOMICS, 2014, 13 (02) :397-406