Chen SH, Kosai K, Xu B, Pham-Nguyen K, Contant C, Finegold MJ, et al.: Combination suicide and cytokine gene therapy for hepatic metastases of colon carcinoma: sustained antitumor immunity prolongs animal survival. Cancer Res 1996, 56:3758–3762.PubMed 30. Yamaguchi A, Goi T, Seki K, Ohtaki N, Maehara M, Kobayashi T, et al.: Clinical significance of combined immunohistochemical detection of CD44v

and sialyl LeX expression for colorectal cancer patients undergoing curative resection. Fludarabine nmr Oncology 1998, 55:400–403.PubMedCrossRef 31. Gotoda T, Matsumura Y, Kondo H, Saitoh D, Shimada Y, Kosuge T, et al.: Expression of CD44 variants and its association with survival PRIMA-1MET cell line in pancreatic cancer. Jpn J Cancer Res 1998, 89:1033–1040.PubMedCrossRef 32. Freeman SM, Ramesh R, Marrogi AJ: Immune system in suicide-gene therapy. Lancet 1997, 349:2–3.PubMedCrossRef Competing interests The authors declare that they have no competing interests. Authors’ contributions SHH, FNR and BHK made conception, designed and coordinated the study, carried out data interpretation, and drafted the manuscript; PZ and HZ participated in the conception and design

of the study, and participated in drafting of manuscript; LJ participated in the design of the study and performed the statistical analysis; XQ and QFY conceived of the study, and participated IWR-1 in its design and coordination and helped to draft the manuscript. All authors read and approved the final manuscript.”
“Background Malignant cells are exposed to Etofibrate a variety of active agents, including hormones, peptide growth factors, cytokines, and many other locally acting substances such as prostaglandins, which together control or modulate the cellular functions. It is of interest to understand the mechanisms by which the

cells integrate signals from different bioactive molecules via their receptors. A notable example is the interaction between pathways from G protein-coupled receptors (GPCRs) and receptor tyrosine kinases (RTKs). Studies in many cells have shown that signals from GPCRs may involve interaction with the epidermal growth factor receptor (EGFR), an ErbB family RTK [1–5]. EGFR, which serves important functions in normal cells [6, 7], is involved in several malignancies [8, 9], and is a target of novel antitumour therapies [10, 11]. In studies including tumour cells from colon and pancreatic cancer, we have found that different mechanisms may be involved in the interaction of pathways from GPCRs and EGFR [12]. EGFR conveys strong mitogenic stimulation in normal hepatocytes [13–16], and several lines of evidence suggest a role of EGFR in hepatocarcinogenesis [17–20]. For example, overexpression of the EGFR agonist transforming growth factor alpha (TGFα) in mice causes hepatic hyperplasia and tumour formation [21, 22], and EGFR is upregulated in a majority of human hepatocarcinomas [23].