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肺癌中的生长抑素受体:从功能到分子成像与治疗

Somatostatin Receptors in Lung Cancer: From Function to Molecular Imaging and Therapeutics.

作者信息

Callison J Clay, Walker Ronald C, Massion Pierre P

机构信息

Division of Allergy, Pulmonary and Critical Care Medicine, Vanderbilt University Medical Center, Tennessee, USA.

Tennessee Valley VA Healthcare System, Tennessee, USA ; Department of Radiology and Radiological Sciences, Vanderbilt University Medical Center, Tennessee, USA ; Vanderbilt-Ingram Cancer Center, Nashville, Tennessee, USA.

出版信息

J Lung Cancer. 2011;10(2):69-76. doi: 10.6058/jlc.2011.10.2.69.

Abstract

Lung cancer is a deadly disease that is difficult to diagnose and even more difficult to treat effectively. Many pathways are known to affect tumor growth, and targeting these pathways provides the cornerstone by which cancer is treated. Somatostatin receptors (SSTR) are a family of G protein coupled receptors that signal to alter hormonal secretion, increase apoptosis, and decrease cellular proliferation. These receptors are expressed in many normal and malignant cells, including both small cell and non-small cell lung cancer. Synthetic analogs of SSTRs are commercially available, but their effects in lung cancer are still largely uncertain. Signaling pathway studies have shown that SSTRs signal through phosphotyrosine phosphatases to induce apoptosis as well as to decrease cell proliferation. Radiolabeled SSTR2 analogs are utilized for radiographic imaging of tumors, which, when combined with positron emission tomography-computed tomography (PET-CT) may improve detection of lung cancer. These radiolabeled SSTR2 analogs also hold promise for targeted chemotherapy as well as radiotherapy. In this review, we summarize what is known about SSTRs and focus our discussion on the knowledge as it relates to lung cancer biology, as well as discuss current and future uses of these receptors for imaging and therapy of lung cancer.

摘要

肺癌是一种致命疾病,难以诊断,更难以有效治疗。已知许多途径会影响肿瘤生长,针对这些途径是治疗癌症的基石。生长抑素受体(SSTR)是一类G蛋白偶联受体,其信号传导可改变激素分泌、增加细胞凋亡并减少细胞增殖。这些受体在许多正常细胞和恶性细胞中表达,包括小细胞肺癌和非小细胞肺癌。SSTR的合成类似物已商业化,但它们在肺癌中的作用仍很大程度上不确定。信号通路研究表明,SSTR通过磷酸酪氨酸磷酸酶发出信号,以诱导细胞凋亡并减少细胞增殖。放射性标记的SSTR2类似物用于肿瘤的放射成像,与正电子发射断层扫描-计算机断层扫描(PET-CT)结合使用时,可能会提高肺癌的检测率。这些放射性标记的SSTR2类似物在靶向化疗以及放射治疗方面也具有前景。在本综述中,我们总结了关于SSTR的已知信息,并将讨论重点放在与肺癌生物学相关的知识上,同时探讨这些受体在肺癌成像和治疗中的当前及未来用途。

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