TY - JOUR
T1 - Primary tumor-derived systemic nANGPTL4 inhibits metastasis
AU - Hübers, Corinne
AU - Abdul Pari, Ashik Ahmed
AU - Grieshober, Denise
AU - Petkov, Martin
AU - Schmidt, Alexander
AU - Messmer, Tatjana
AU - Heyer, Christian Moritz
AU - Schölch, Sebastian
AU - Kapel, Stephanie S.
AU - Gengenbacher, Nicolas
AU - Singhal, Mahak
AU - Schieb, Benjamin
AU - Fricke, Claudine
AU - Will, Rainer
AU - Remans, Kim
AU - Utikal, Jochen Sven
AU - Reissfelder, Christoph
AU - Schlesner, Matthias
AU - Hodivala-Dilke, Kairbaan M.
AU - Kersten, Sander
AU - Goerdt, Sergij
AU - Augustin, Hellmut G.
AU - Felcht, Moritz
PY - 2023/1/2
Y1 - 2023/1/2
N2 - Primary tumors and distant site metastases form a bidirectionally communicating system. Yet, the molecular mechanisms of this crosstalk are poorly understood. Here, we identified the proteolytically cleaved fragments of angiopoietin-like 4 (ANGPTL4) as contextually active protumorigenic and antitumorigenic contributors in this communication ecosystem. Preclinical studies in multiple tumor models revealed that the C-terminal fragment (cANGPTL4) promoted tumor growth and metastasis. In contrast, the N-terminal fragment of ANGPTL4 (nANGPTL4) inhibited metastasis and enhanced overall survival in a postsurgical metastasis model by inhibiting WNT signaling and reducing vascularity at the metastatic site. Tracing ANGPTL4 and its fragments in tumor patients detected full-length ANGPTL4 primarily in tumor tissues, whereas nANGPTL4 predominated in systemic circulation and correlated inversely with disease progression. The study highlights the spatial context of the proteolytic cleavage-dependent pro- and antitumorigenic functions of ANGPTL4 and identifies and validates nANGPTL4 as a novel biomarker of tumor progression and antimetastatic therapeutic agent.
AB - Primary tumors and distant site metastases form a bidirectionally communicating system. Yet, the molecular mechanisms of this crosstalk are poorly understood. Here, we identified the proteolytically cleaved fragments of angiopoietin-like 4 (ANGPTL4) as contextually active protumorigenic and antitumorigenic contributors in this communication ecosystem. Preclinical studies in multiple tumor models revealed that the C-terminal fragment (cANGPTL4) promoted tumor growth and metastasis. In contrast, the N-terminal fragment of ANGPTL4 (nANGPTL4) inhibited metastasis and enhanced overall survival in a postsurgical metastasis model by inhibiting WNT signaling and reducing vascularity at the metastatic site. Tracing ANGPTL4 and its fragments in tumor patients detected full-length ANGPTL4 primarily in tumor tissues, whereas nANGPTL4 predominated in systemic circulation and correlated inversely with disease progression. The study highlights the spatial context of the proteolytic cleavage-dependent pro- and antitumorigenic functions of ANGPTL4 and identifies and validates nANGPTL4 as a novel biomarker of tumor progression and antimetastatic therapeutic agent.
U2 - 10.1084/jem.20202595
DO - 10.1084/jem.20202595
M3 - Article
C2 - 36269299
AN - SCOPUS:85140417639
SN - 0022-1007
VL - 220
JO - The Journal of experimental medicine
JF - The Journal of experimental medicine
IS - 1
ER -