Currently, there are no reliable diagnostic biomarkers for the early detection of ovarian cancer in humans. Advanced proteomics technology now exists to comprehensively investigate and discover diagnostic biomarkers in complex biological samples such as plasma and tissue. However, a major barrier to identifying candidate biomarkers in human ovarian cancer has been a lack of suitable patient samples from which to study. The domestic hen has emerged as one of the few animal models for ovarian cancer due to its spontaneous formation of tumors at two years of age. This predictability along with the widespread availability of animal specimens makes the hen a viable model for studying the onset and progression of ovarian cancer. Herein we propose to study the domestic hen proteome as a function of time using advanced mass spectrometry and proteomics technology to elucidate candidate biomarkers predicative of ovarian cancer. The ultimate goal is to translate these findings into human ovarian cancer where biological variability is much higher. During the course of this proposal, the principal investigator will be trained in multiple areas of biological sciences in an effort to transition him into an independent scientist. Public Description of Research Project. Ovarian cancer is a devastating disease that goes mostly undetected until the advanced stages where survival rates are poor. Early diagnostic tests are desperately needed to curb the mortality rates from ovarian cancer. This proposal seeks to identify blood-borne protein biomarkers that can be used for early diagnosis in ovarian cancer patients.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Mentored Quantitative Research Career Development Award (K25)
Project #
5K25CA128666-03
Application #
7669386
Study Section
Subcommittee G - Education (NCI)
Program Officer
Jakowlew, Sonia B
Project Start
2007-08-15
Project End
2012-07-31
Budget Start
2009-08-01
Budget End
2010-07-31
Support Year
3
Fiscal Year
2009
Total Cost
$143,370
Indirect Cost
Name
North Carolina State University Raleigh
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
042092122
City
Raleigh
State
NC
Country
United States
Zip Code
27695
Nepomuceno, Angelito I; Shao, Huanjie; Jing, Kai et al. (2015) In-depth LC-MS/MS analysis of the chicken ovarian cancer proteome reveals conserved and novel differentially regulated proteins in humans. Anal Bioanal Chem 407:6851-63
Hawkridge, Adam M (2014) The chicken model of spontaneous ovarian cancer. Proteomics Clin Appl 8:689-99
Andrews Kingon, Genna L; Petitte, James N; Muddiman, David C et al. (2013) Multi-peptide nLC-PC-IDMS-SRM-based assay for the quantification of biomarkers in the chicken ovarian cancer model. Methods 61:323-30
Dixon, R Brent; Bereman, Michael S; Petitte, James N et al. (2011) One-Year Plasma N-linked Glycome Intra-individual and Inter-individual Variability in the Chicken Model of Spontaneous Ovarian Adenocarcinoma. Int J Mass Spectrom 305:79-86
Andrews, Genna L; Dean, Ralph A; Hawkridge, Adam M et al. (2011) Improving proteome coverage on a LTQ-Orbitrap using design of experiments. J Am Soc Mass Spectrom 22:773-83
Andrews, Genna L; Simons, Brigitte L; Young, J Bryce et al. (2011) Performance characteristics of a new hybrid quadrupole time-of-flight tandem mass spectrometer (TripleTOF 5600). Anal Chem 83:5442-6
Hawkridge, Adam M; Wysocky, Rebecca B; Petitte, James N et al. (2010) Measuring the intra-individual variability of the plasma proteome in the chicken model of spontaneous ovarian adenocarcinoma. Anal Bioanal Chem 398:737-49
Hawkridge, Adam M; Muddiman, David C (2009) Mass spectrometry-based biomarker discovery: toward a global proteome index of individuality. Annu Rev Anal Chem (Palo Alto Calif) 2:265-77
Dixon, R Brent; Sampson, Jason S; Hawkridge, Adam M et al. (2008) Ambient aerodynamic ionization source for remote analyte sampling and mass spectrometric analysis. Anal Chem 80:5266-71