Tran Phu, Nguyen Cham, Klempner Samuel J
Division of Hematology-Oncology, University of California Irvine, Orange, CA, USA.
Department of Pharmacy, University of California Irvine, Orange, CA, USA.
Int Neurourol J. 2016 Nov;20(Suppl 2):S131-140. doi: 10.5213/inj.1632740.370. Epub 2016 Nov 22.
Phosphatidylinositol-3-kinase (PI3K) pathway signaling is an established oncogenic signal transduction pathway implicated in multiple malignancies. Therapeutic targeting of PI3K pathway components has improved outcomes in chronic lymphocytic leukemia, kidney cancer, breast cancer, and neuroendocrine tumors. Gastric cancers harbor some of the highest rates of oncogenic alterations in PI3K but attempts to translate this genomic observation have met with limited clinical success and novel approaches are needed. In the following review we discuss PI3K signaling, previous preclinical and clinical investigations in gastric cancer, and discuss future strategies aimed at overcoming resistance and improving efficacy. Identification and refinement of molecular tumor subtypes, development of predictive biomarkers along, and rational drug combination strategies are key to capitalizing on the therapeutic potential of PI3K pathway directed therapies in gastric cancers.
磷脂酰肌醇-3-激酶(PI3K)信号通路是一种已确定的致癌信号转导通路,与多种恶性肿瘤有关。针对PI3K通路成分的治疗靶点已改善了慢性淋巴细胞白血病、肾癌、乳腺癌和神经内分泌肿瘤的治疗结果。胃癌中PI3K致癌改变的发生率较高,但将这一基因组学观察结果转化为临床应用的尝试取得的临床成功有限,因此需要新的方法。在以下综述中,我们将讨论PI3K信号传导、先前在胃癌中的临床前和临床研究,并探讨旨在克服耐药性和提高疗效的未来策略。识别和细化分子肿瘤亚型、开发预测性生物标志物以及合理的联合用药策略,是充分利用PI3K通路定向治疗在胃癌中的治疗潜力的关键。