PMID- 9798673 OWN - NLM STAT- MEDLINE DCOM- 19981119 LR - 20191102 IS - 0950-9232 (Print) IS - 0950-9232 (Linking) VI - 17 IP - 16 DP - 1998 Oct 22 TI - Evidence for a role of Met-HGF/SF during Ras-mediated tumorigenesis/metastasis. PG - 2019-25 AB - Aberrations in Met-hepatocyte growth factor/scatter factor (HGF/SF) signaling have been implicated in the acquisition of tumorigenic and metastatic phenotypes. Here we show that murine NIH3T3 and C127 cells transformed by the Ras oncogene overexpress the Met receptor, resulting in enhanced HGF/SF-mediated responses in vitro including invasion through basement membrane. Accompanying the increase in Met in ras-transformed NIH3T3 cells, there is a decrease in endogenous HGF/SF expression as previously observed in cells exogenously overexpressing Met. However, subcutaneously grown tumors and experimental lung metastases derived from these cells express significantly higher levels of endogenous HGF/SF together with high levels of Met. These results suggest Met-HGF/SF signaling enhances tumor growth and metastasis of Ras-transformed NIH3T3 cells. FAU - Webb, C P AU - Webb CP AD - ABL-Basic Research Program, NCI-Frederick Cancer Research and Development Center, Maryland 21702, USA. FAU - Taylor, G A AU - Taylor GA FAU - Jeffers, M AU - Jeffers M FAU - Fiscella, M AU - Fiscella M FAU - Oskarsson, M AU - Oskarsson M FAU - Resau, J H AU - Resau JH FAU - Vande Woude, G F AU - Vande Woude GF LA - eng GR - N01-CO-46000/CO/NCI NIH HHS/United States PT - Journal Article PT - Research Support, U.S. Gov't, P.H.S. PL - England TA - Oncogene JT - Oncogene JID - 8711562 RN - EC 2.7.10.1 (Proto-Oncogene Proteins c-met) RN - EC 3.6.5.2 (Oncogene Protein p21(ras)) SB - IM MH - 3T3 Cells MH - Animals MH - Cell Line MH - Cell Line, Transformed MH - *Cell Transformation, Neoplastic MH - Dogs MH - Female MH - Humans MH - Lung Neoplasms/secondary MH - Mice MH - Mice, Knockout MH - Mice, Nude MH - Oncogene Protein p21(ras)/genetics/*metabolism MH - Proto-Oncogene Proteins c-met/biosynthesis/*physiology EDAT- 1998/11/03 00:00 MHDA- 1998/11/03 00:01 CRDT- 1998/11/03 00:00 PHST- 1998/11/03 00:00 [pubmed] PHST- 1998/11/03 00:01 [medline] PHST- 1998/11/03 00:00 [entrez] AID - 10.1038/sj.onc.1202135 [doi] PST - ppublish SO - Oncogene. 1998 Oct 22;17(16):2019-25. doi: 10.1038/sj.onc.1202135.