Role of Paxillin in Lung Cancer

描述(申请人提供)：肺癌是一种毁灭性的疾病，总体存活率很低。为了对这种疾病产生重大影响，必须确定新的目标和机制。肺癌的一个特征是细胞运动性增强、迁移、侵袭和早期转移到淋巴结和其他器官。细胞骨架，特别是以肌动蛋白为基础的，本质上参与了肺癌的这些生物学功能。我们以前已经证明，焦点粘连受到各种癌基因转化的显著影响，尤其是在肺癌中。尤其是在非小细胞肺癌(NSCLC)中，68 kDa的粘着斑蛋白Paxlin被显著改变(过度表达并通过磷酸化激活)。在初步数据中，我们首次发现在非小细胞肺癌中存在paxlin基因的体细胞突变。例如，在大细胞癌中，突变频率高达18%。肺癌的不同组织在突变频率上存在差异。突变位于LD结构域(对结合其他分子如FAK很重要)和LIM结构域(对肌动蛋白结合重要的锌指结构域)之间。此外，在非裔美国人、高加索人和台湾人的肺癌样本中，paxlin基因突变也存在差异。巴西林最常见的突变是A127T，它能提高肺癌细胞存活率、体内肿瘤生长以及增强血管生成。利用双向PAGE，突变体A127T也导致了H522 NSCLC细胞与野生型巴西林相比蛋白质表达的差异。我们还发现了一组扩增了paxlin基因的非小细胞肺癌。肺癌中受体酪氨酸激酶c-Met的激活也会导致帕西林的磷酸化。有趣的是，在一些A127T突变的细胞系中，存在c-Met(R988C，膜旁结构域)突变。根据我们的最新发现，我们将提出以下目标：1.确定Paxlin在非小细胞肺癌中的表达、扩增和突变，并与人口学和临床因素、相关生物标记物(如c-Met)和患者生存相关；2.确定Paxlin和突变Paxlin在NSCLC中的生物学功能。同时，确定对肺癌的治疗抑制作用的可能性；3.确定帕西林和c-Met在非小细胞肺癌生物学功能、血管生成和转移中的联合作用。在进行这些研究时，我们将得出转化、转移和最终治疗肺癌的新机制。公共卫生相关性：肺癌是一种毁灭性的疾病，转移频繁，对治疗反应差。我们已经确定细胞骨架蛋白Paxlin在肺癌中起重要作用，特别是与细胞运动/迁移和最终转移有关。我们还发现，在肺癌中可以选择性地突变和/或扩增paxlin基因，从而使其更具侵袭性。我们的目标是研究帕西林在肺癌中的作用，并最终得出针对这种难治疾病的新疗法。

DESCRIPTION (provided by applicant): Lung cancer is a devastating illness with a poor overall survival. In order to dramatically impact on this disease, new targets and mechanisms have to be identified. One hallmark of lung cancer is enhanced cell motility, migration, invasion and early metastasis to lymph nodes and other organs. The cytoskeleton, especially actin-based, is intrinsically involved in these biological functions of lung cancer. We have previously shown that the focal adhesion is dramatically affected by transformation by various oncogenes, especially in lung cancer. In particular, the 68 kDa focal adhesion protein paxillin is dramatically altered (over-expressed and activated through phosphorylation) in non-small cell lung cancer (NSCLC). In preliminary data, we show for the first time that there are somatic mutations of the paxillin gene in NSCLC. In large cell carcinoma, for example, mutational frequency is up to 18%. There are differences in the mutational frequencies for the various histologies of lung cancer. The mutations were localized in between the LD domains (important for binding other molecules such as FAK) and in the LIM domains (zinc finger domains important in actin binding). Also, there were differences in paxillin gene mutations in lung cancer samples from African Americans, Caucasians, and Taiwanese. The most frequent mutation of paxillin, A127T, lead to enhanced lung cancer cell survival, tumor growth in vivo as well as enhanced angiogenesis. Using two-dimensional PAGE, the mutant A127T also led to differential protein expression in H522 NSCLC cells as compared to wild-type paxillin. We have also identified a subset of NSCLC that have amplification of the paxillin gene. Paxillin also was phosphorylated in response to activation of the receptor tyrosine kinase c-Met in lung cancer. Interestingly, in some cell lines with A127T mutation, there was a mutation of c-Met (R988C, juxtamembrane domain). Based on our most recent findings, we would propose the following aims: 1. Determine the expression, amplification, and mutations of paxillin in NSCLC and correlate with demographic and clinical factors, pertinent biological markers (such as c-Met) and patient survival; 2. Determine the biological functions of paxillin and mutated paxillin in NSCLC. Also, determine the potential for therapeutic inhibition in lung cancer; 3. Determine the combined role of paxillin and c-Met in NSCLC biological functions, angiogenesis and metastasis. In performing these studies, we will have arrived at novel mechanisms for transformation, metastasis and ultimately therapy against lung cancer. PUBLIC HEALTH RELEVANCE: Lung cancer is a devastating illness with frequent metastases and poor response to therapy. We have determined that the cytoskeletal protein paxillin plays an important role in lung cancer, especially as related to cell motility/migration with ultimate metastasis. We have also identified that paxillin gene can be selectively mutated and/or amplified in lung cancer and thereby make them more aggressive. Our goal is to study the role of paxillin in lung cancer and ultimately arrive at novel therapy against this difficult disease.