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Journal Thoracic Oncology

WCLC2016-Abstract-Book_vF-WEB_revNov17-1

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Abstracts <strong>Journal</strong> of <strong>Thoracic</strong> <strong>Oncology</strong> • Volume 12 Issue S1 January 2017<br />

Background: The youthful lung cancer may constitute an entity with distinct<br />

clinicopathologic characteristics. The serine/threonine kinase LKB1, also<br />

known as Serine/Threonine Kinase 11-STK11, is a known tumor suppressor<br />

gene involved in cellular responses such as energy metabolism, cell polarity<br />

and cell growth, but the role of LKB1 pathway in lung adenocarcinoma (ADC) is<br />

barely studied, especially in young patients. Methods: Fifty lung ADC patients<br />

were retrospectively analysed. After RNA purification from formalin fixed<br />

and paraffin embedded tumor tissues, we analysed the mRNA expression<br />

levels of LKB1 and of genes involved in its pathway, such as cyclin D1 (CCND1),<br />

beta catenin (CCNNB1), lysyl oxidase (LOX), yes-associated protein-1 (YAP-1),<br />

and survivin, with NanoString technology, a new tool for a more accurate<br />

expression profiling. KRAS mutations were investigated by pyrosequencing<br />

analysis. Clinicopathologic characteristics and survival analysis were<br />

available for all patients. Results: Patients under 50 years old (including 50)<br />

were defined as the younger group and patients above 50 years old were<br />

defined as the older group. Among all the clinicopathologic characteristics,<br />

in the younger group there were more women, less solid and more acinar<br />

adenocarcinoma prevalent pattern in comparison to the older group. Younger<br />

and older groups showed similar survival rates, as well as KRAS mutations<br />

frequencies. Also, in the comparison between the gene expression level of the<br />

analyzed genes and the two different age subgroups,no statistical difference<br />

was found. We then focused on the LKB1 pathway in all series, independently<br />

from the age stratification, founding LKB1 low expression associated with<br />

low cyclin D1 (CCND1) (p

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