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. Author manuscript; available in PMC: 2011 Jun 1.
Published in final edited form as: Cancer Res. 2008 Dec 1;68(23):9996–10003. doi: 10.1158/0008-5472.CAN-08-2492

Figure 2.

Figure 2

MGC4-2 with altered morphology and cytogenetics was more inductive than MGLN and MGRWV in chimeric prostate tumor growth in mice. A, chimeric C4-2-Luc tumors produced by coinjecting with MGC4-2 grew significantly faster than those from MGRWV, MGLN, or in the absence of MG cells (columns, mean of tumor volume of five independent measurements; bars, SE). C4-2-Luc alone failed to form tumors in mice (A). These data agree with serum PSA (B) and chimeric tumor epithelial cell-associated luciferase activity (C).