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Editorial
. 2010 Jan;17(1):14-7.
doi: 10.1245/s10434-009-0766-0. Epub 2009 Oct 20.

Targeting gastric cancer with trastuzumab: new clinical practice and innovative developments to overcome resistance

Editorial

Targeting gastric cancer with trastuzumab: new clinical practice and innovative developments to overcome resistance

Dimitrios H Roukos. Ann Surg Oncol. 2010 Jan.
No abstract available

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Figures

Fig. 1
Fig. 1
a Ligand binding and subsequent Erbb dimer formation initiates signaling through a complex array of intracellular pathways that initiate and control a range of cellular processes. Dimer formation results in the cross-phosphorylation of the dimer partners, creating docking sites that allow the recruitment of downstream signaling components and the formation of signaling complexes. Two key signaling pathways activated by the Erbb family dimers are the MAPK pathway, which stimulates proliferation, and the PI3K–Akt pathway, which promotes tumor cell survival (see the figure). Only signaling through these two pathways and some of the known outcomes are shown here for simplicity. b The antibody trastuzumab binds directly to domain IV of the extracellular region of ERBB2, suppressing ERBB2 signaling activity, preventing cleavage of the extracellular domain, and marking tumor cells that overexpress ERBB2 for further immunological attack through antibody-dependent cell-mediated cytotoxicity. GSK3β, glycogen synthase kinase 3β; NF-κB, nuclear factor-κB; PDK1, pyruvate dehydrogenase kinase 1; PIP2, phosphatidylinositol biphosphate; PIP3, phosphatidylinositol triphosphate

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