Evelyn Chris R, Wade Susan M, Wang Qin, Wu Mei, Iñiguez-Lluhí Jorge A, Merajver Sofia D, Neubig Richard R
Department of Pharmacology, University of Michigan Medical Center, 1301 MSRB III, Room 2220D, 1150 West Medical Center Drive, Ann Arbor, MI 48109-0632, USA.
Mol Cancer Ther. 2007 Aug;6(8):2249-60. doi: 10.1158/1535-7163.MCT-06-0782.
Lysophosphatidic acid receptors stimulate a Galpha(12/13)/RhoA-dependent gene transcription program involving the serum response factor (SRF) and its coactivator and oncogene, megakaryoblastic leukemia 1 (MKL1). Inhibitors of this pathway could serve as useful biological probes and potential cancer therapeutic agents. Through a transcription-based high-throughput serum response element-luciferase screening assay, we identified two small-molecule inhibitors of this pathway. Mechanistic studies on the more potent CCG-1423 show that it acts downstream of Rho because it blocks SRE.L-driven transcription stimulated by Galpha(12)Q231L, Galpha(13)Q226L, RhoA-G14V, and RhoC-G14V. The ability of CCG-1423 to block transcription activated by MKL1, but not that induced by SRF-VP16 or GAL4-VP16, suggests a mechanism targeting MKL/SRF-dependent transcriptional activation that does not involve alterations in DNA binding. Consistent with its role as a Rho/SRF pathway inhibitor, CCG-1423 displays activity in several in vitro cancer cell functional assays. CCG-1423 potently (<1 mumol/L) inhibits lysophosphatidic acid-induced DNA synthesis in PC-3 prostate cancer cells, and whereas it inhibits the growth of RhoC-overexpressing melanoma lines (A375M2 and SK-Mel-147) at nanomolar concentrations, it is less active on related lines (A375 and SK-Mel-28) that express lower levels of Rho. Similarly, CCG-1423 selectively stimulates apoptosis of the metastasis-prone, RhoC-overexpressing melanoma cell line (A375M2) compared with the parental cell line (A375). CCG-1423 inhibited Rho-dependent invasion by PC-3 prostate cancer cells, whereas it did not affect the Galpha(i)-dependent invasion by the SKOV-3 ovarian cancer cell line. Thus, based on its profile, CCG-1423 is a promising lead compound for the development of novel pharmacologic tools to disrupt transcriptional responses of the Rho pathway in cancer.
溶血磷脂酸受体刺激一种依赖Gα(12/13)/RhoA的基因转录程序,该程序涉及血清反应因子(SRF)及其共激活因子和癌基因——巨核细胞白血病1(MKL1)。该信号通路的抑制剂可作为有用的生物学探针和潜在的癌症治疗药物。通过基于转录的高通量血清反应元件-荧光素酶筛选试验,我们鉴定出了该信号通路的两种小分子抑制剂。对更有效的CCG-1423进行的机制研究表明,它作用于Rho的下游,因为它能阻断由Gα(12)Q231L、Gα(13)Q226L、RhoA-G14V和RhoC-G14V刺激的SRE.L驱动的转录。CCG-1423能够阻断由MKL1激活的转录,但不能阻断由SRF-VP16或GAL4-VP16诱导的转录,这表明其作用机制是靶向MKL/SRF依赖的转录激活,而不涉及DNA结合的改变。与其作为Rho/SRF信号通路抑制剂的作用一致,CCG-1423在几种体外癌细胞功能试验中显示出活性。CCG-1423能有效(<1 μmol/L)抑制溶血磷脂酸诱导的PC-3前列腺癌细胞中的DNA合成,并且它在纳摩尔浓度下能抑制过表达RhoC的黑色素瘤细胞系(A375M2和SK-Mel-147)的生长,但对表达较低水平Rho的相关细胞系(A375和SK-Mel-28)活性较低。同样,与亲代细胞系(A375)相比,CCG-1423能选择性地刺激易于转移、过表达RhoC的黑色素瘤细胞系(A375M2)的凋亡。CCG-1423抑制PC-3前列腺癌细胞的Rho依赖性侵袭,而不影响SKOV-3卵巢癌细胞系的Gα(i)依赖性侵袭。因此,基于其特性,CCG-1423是一种有前景的先导化合物,可用于开发新型药理学工具,以破坏癌症中Rho信号通路的转录反应。