TY - JOUR
T1 - Synthetic analogues of migrastatin that inhibit mammary tumor metastasis in mice
AU - Shan, Dandan
AU - Chen, Lin
AU - Njardarson, Jon T.
AU - Gaul, Christoph
AU - Ma, Xiaojing
AU - Danishefsky, Samuel J.
AU - Huang, Xin Yun
PY - 2005/3/8
Y1 - 2005/3/8
N2 - Tumor metastasis is the most common cause of death in cancer patients. Here, we show that two, fully synthetic migrastatin analogues, core macroketone and core macrolactam, are potent inhibitors of metastasis in a murine breast tumor model. Administration of these readily accessible compounds nearly completely inhibits lung metastasis of highly metastatic mammary carcinoma cells. Treatment of tumor cells with core macroketone and core macrolactam blocks Rac activation, lamellipodia formation, and cell migration, suggesting that these chemical compounds interfere with the invasion step of the metastatic process. These compounds also inhibit the migration of human metastatic breast cancer cells, prostate cancer cells, and colon cancer cells but not normal mammary-gland epithelial cells, fibroblasts, and leukocytes. These data demonstrate that the macroketone and macrolactam core structures are specific small-molecule inhibitors of tumor metastasis. These compounds or their analogues could potentially be used in cancer-therapy strategies.
AB - Tumor metastasis is the most common cause of death in cancer patients. Here, we show that two, fully synthetic migrastatin analogues, core macroketone and core macrolactam, are potent inhibitors of metastasis in a murine breast tumor model. Administration of these readily accessible compounds nearly completely inhibits lung metastasis of highly metastatic mammary carcinoma cells. Treatment of tumor cells with core macroketone and core macrolactam blocks Rac activation, lamellipodia formation, and cell migration, suggesting that these chemical compounds interfere with the invasion step of the metastatic process. These compounds also inhibit the migration of human metastatic breast cancer cells, prostate cancer cells, and colon cancer cells but not normal mammary-gland epithelial cells, fibroblasts, and leukocytes. These data demonstrate that the macroketone and macrolactam core structures are specific small-molecule inhibitors of tumor metastasis. These compounds or their analogues could potentially be used in cancer-therapy strategies.
KW - Cancer therapy
KW - Cell migration
KW - Chemical biology
UR - http://www.scopus.com/inward/record.url?scp=14844343474&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=14844343474&partnerID=8YFLogxK
U2 - 10.1073/pnas.0500658102
DO - 10.1073/pnas.0500658102
M3 - Article
C2 - 15728385
AN - SCOPUS:14844343474
SN - 0027-8424
VL - 102
SP - 3772
EP - 3776
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 10
ER -