Group XIV C-type lectins: emerging targets in tumor angiogenesis

被引:4
作者
Yee, Elliott J. [1 ]
Vigil, Isaac [1 ]
Sun, Yi [1 ]
Torphy, Robert J. [2 ]
Schulick, Richard D. [1 ]
Zhu, Yuwen [1 ]
机构
[1] Univ Colorado Anschutz Med Campus, Dept Surg, 12800 E 19th Ave,RC1 North,P18-8116, Aurora, CO 80045 USA
[2] Mem Sloan Kettering Canc Ctr, Dept Surg, New York, NY USA
基金
美国国家卫生研究院;
关键词
Tumor angiogenesis; C-type lectin; Vessel normalization; Immunotherapy; HEREDITARY HEMORRHAGIC TELANGIECTASIA; KINASE; ALK1; ARTERIOVENOUS-MALFORMATIONS; FUNCTIONAL-ANALYSIS; NOTCH; MUTATIONS; BMP9; EXPRESSION; IDENTIFICATION; MECHANISMS;
D O I
10.1007/s10456-024-09907-x
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
C-type lectins, distinguished by a C-type lectin binding domain (CTLD), are an evolutionarily conserved superfamily of glycoproteins that are implicated in a broad range of physiologic processes. The group XIV subfamily of CTLDs are comprised of CD93, CD248/endosialin, CLEC14a, and thrombomodulin/CD141, and have important roles in creating and maintaining blood vessels, organizing extracellular matrix, and balancing pro- and anti-coagulative processes. As such, dysregulation in the expression and downstream signaling pathways of these proteins often lead to clinically relevant pathology. Recently, group XIV CTLDs have been shown to play significant roles in cancer progression, namely tumor angiogenesis and metastatic dissemination. Interest in therapeutically targeting tumor vasculature is increasing and the search for novel angiogenic targets is ongoing. Group XIV CTLDs have emerged as key moderators of tumor angiogenesis and metastasis, thus offering substantial therapeutic promise for the clinic. Herein, we review our current knowledge of group XIV CTLDs, discuss each's role in malignancy and associated potential therapeutic avenues, briefly discuss group XIV CTLDs in the context of two other relevant lectin families, and offer future direction in further elucidating mechanisms by which these proteins function and facilitate tumor growth.
引用
收藏
页码:173 / 192
页数:20
相关论文
共 127 条
[1]   Successful In Vitro Expansion and Differentiation of Cord Blood Derived CD34+Cells into Early Endothelial Progenitor Cells Reveals Highly Differential Gene Expression [J].
Ahrens, Ingo ;
Domeij, Helena ;
Topcic, Denijal ;
Haviv, Izhak ;
Merivirta, Ruusu-Maaria ;
Agrotis, Alexander ;
Leitner, Ephraem ;
Jowett, Jeremy B. ;
Bode, Christoph ;
Lappas, Martha ;
Peter, Karlheinz .
PLOS ONE, 2011, 6 (08)
[2]   Vascular Mechanobiology - Endothelial Cell Responses to Fluid Shear Stress - [J].
Ando, Joji ;
Yamamoto, Kimiko .
CIRCULATION JOURNAL, 2009, 73 (11) :1983-1992
[3]   AtezoTRIBE: a randomised phase II study of FOLFOXIRI plus bevacizumab alone or in combination with atezolizumab as initial therapy for patients with unresectable metastatic colorectal cancer [J].
Antoniotti, Carlotta ;
Borelli, Beatrice ;
Rossini, Daniele ;
Pietrantonio, Filippo ;
Morano, Federica ;
Salvatore, Lisa ;
Lonardi, Sara ;
Marmorino, Federica ;
Tamberi, Stefano ;
Corallo, Salvatore ;
Tortora, Giampaolo ;
Bergamo, Francesca ;
Brunella, Di Stefano ;
Boccaccino, Alessandra ;
Grassi, Elisa ;
Racca, Patrizia ;
Tamburini, Emiliano ;
Aprile, Giuseppe ;
Moretto, Roberto ;
Boni, Luca ;
Falcone, Alfredo ;
Cremolini, Chiara .
BMC CANCER, 2020, 20 (01)
[4]   Targeting Metabolism to Improve the Tumor Microenvironment for Cancer Immunotherapy [J].
Bader, Jackie E. ;
Voss, Kelsey ;
Rathmell, Jeffrey C. .
MOLECULAR CELL, 2020, 78 (06) :1019-1033
[5]   Circulating galectin-1 delineates response to bevacizumab in melanoma patients and reprograms endothelial cell biology [J].
Bannoud, Nadia ;
Stupirski, Juan C. ;
Cagnoni, Alejandro J. ;
Hockl, Pablo F. ;
Saez, Juan M. Perez ;
Garcia, P. Alfredo ;
Mahmoud, Yamil D. ;
Tudela, Julian Gambarte ;
Scheidegger, Marco A. ;
Marshall, Andrea ;
Corrie, Pippa G. ;
Middleton, Mark R. ;
Marino, Karina, V ;
Girotti, M. Romina ;
Croci, Diego O. ;
Rabinovich, Gabriel A. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2023, 120 (03)
[6]   Soluble CD93 is an apoptotic cell opsonin recognized by αxβ2 [J].
Blackburn, Jack W. D. ;
Lau, Darius H. C. ;
Liu, Elaine Y. ;
Ellins, Jessica ;
Vrieze, Angela M. ;
Pawlak, Emily N. ;
Dikeakos, Jimmy D. ;
Heit, Bryan .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2019, 49 (04) :600-610
[7]   Human IgG1 antibodies suppress angiogenesis in a target-independent manner [J].
Bogdanovich, Sasha ;
Kim, Younghee ;
Mizutani, Takeshi ;
Yasuma, Reo ;
Tudisco, Laura ;
Cicatiello, Valeria ;
Bastos-Carvalho, Ana ;
Kerur, Nagaraj ;
Hirano, Yoshio ;
Baffi, Judit Z. ;
Tarallo, Valeria ;
Li, Shengjian ;
Yasuma, Tetsuhiro ;
Arpitha, Parthasarathy ;
Fowler, Benjamin J. ;
Wright, Charles B. ;
Apicella, Ivana ;
Greco, Adelaide ;
Brunetti, Arturo ;
Ruvo, Menotti ;
Sandomenico, Annamaria ;
Nozaki, Miho ;
Ijima, Ryo ;
Kaneko, Hiroki ;
Ogura, Yuichiro ;
Terasaki, Hiroko ;
Ambati, Balamurali K. ;
Leusen, Jeanette H. W. ;
Langdon, Wallace Y. ;
Clark, Michael R. ;
Armour, Kathryn L. ;
Bruhns, Pierre ;
Verbeek, J. Sjef ;
Gelfand, Bradley D. ;
De Falco, Sandro ;
Ambati, Jayakrishna .
SIGNAL TRANSDUCTION AND TARGETED THERAPY, 2016, 1
[8]   CD93 is rapidly shed from the surface of human myeloid cells and the soluble form is detected in human plasma [J].
Bohlson, SS ;
Silva, R ;
Fonseca, MI ;
Tenner, AJ .
JOURNAL OF IMMUNOLOGY, 2005, 175 (02) :1239-1247
[9]   C-type lectin family XIV members and angiogenesis [J].
Borah, Supriya ;
Vasudevan, Dileep ;
Swain, Rajeeb K. .
ONCOLOGY LETTERS, 2019, 18 (04) :3954-3962
[10]   Circulating Thrombomodulin: Release Mechanisms, Measurements, and Levels in Diseases and Medical Procedures [J].
Boron, Mallorie ;
Hauzer-Martin, Tiffany ;
Keil, Joseph ;
Sun, Xue-Long .
TH OPEN, 2022, 06 (03) :e194-e212