Lung Cancer


 WCCRB-2018

Scientific Federation invites all the participants from all over the world to attend 2nd World Congress on Clinical Research & Biomarkers during September 17-18, 2018 Toronto, Canada.
Now a day’s cancer is very dangerous disease and an especially lung cancer plays major role. Blood based biomarkers have potential in cancer screening and their role could extend further from general population risk assessment to treatment response evaluation and recurrence monitoring. The rich content of diverse cellular and molecular elements in blood, which provide information about the health status of an individual, makes it an ideal compartment to develop noninvasive diagnostics for cancer. Other common cancers, notably breast and lung cancer, lack established biomarkers with demonstrated clinical utility in a screening setting. There is a need for biomarkers with the required sensitivity and specificity for the detection of frequently occurring cancer types. Protein markers currently in clinical use, which include Cancer antigen 125 for ovarian cancer, Carbohydrate antigen 199 for pancreatic cancer, Carcino embryonic antigen for colon cancer and Prostate specific antigen for prostate cancer, have limitations with respect to their use for screening owing to low sensitivity and specificity in early stages and inability to distinguish aggressive from indolent tumors.
This is significantly more sensitive than the most sensitive detection methods from electrophoretic gels with silver staining or fluorescence staining, or the general mass spectrometry methods. Secondly, it is known that many proteins have post-translational modifications (PTMs) and splice variants; these different forms of the same gene product may have different functions/enzyme activities and play very different roles in biology. However the important information on the impact of PTM and protein splicing is lost in the antibody, LC-MS or gel-based analysis because these platforms cannot directly measure the functional features of the proteome. The introduction of exogenous protein(s) from the PEP samples could potentially supersede any rate-limiting protein function and enhance the hexokinase activity. As such, this assay may also detect the effect of proteins from other pathways that cross-interact with the glycol tic pathway.


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