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Page 33

Biochemistry & Molecular Biology Journal

ISSN: 2471-8084

Internat i ona l Conference on

Biotechnology, Biomarkers

& Systems Biology

M a r c h 0 4 - 0 5 , 2 0 1 9

Am s t e r d a m , N e t h e r l a n d s

Biotechnology, Biomarkers & Systems Biology 2019

E

arly work uncovered HCG1745306 isoform CRA-a, and histone H1.2 as

potential specific plasma biomarkers for the identification of patients with

early ER

+

(estrogen receptor-positive) breast cancer. However, while these

markers were absent in controls, the results were obtained from only two

patients and therefore require verification in a larger patient cohort. Moreover,

in another preliminary study, we identified potential extracellular vesicles

(EV) factors which might serve as biomarkers for predictive and diagnostic

purposes in metastatic breast cancer. Plasma samples from seven different

metastatic and non-metastatic ER

+

breast cancer patients were collected,

EV were isolated and their protein content analyzed by mass spectrometry

and FunRich analysis. In this study, we found several putative plasma EV

biomarkers for metastatic ER

+

breast cancer prediction and diagnosis, such

as serum amyloid A1, known to promote widespread metastasis in a breast

cancer animal model. In conjunction with academic and clinical colleagues

from the Department of Biomedical Sciences at the University of Hull and

Castle Hill Hospital, we propose to examine the pathophysiological role of the

proteins found in the original works using tissue samples from patients with

a confirmed diagnosis of breast cancer compared to adjacent benign breast

tissues. If the initial results are confirmed, we will determine if these markers

can be identified in whole blood samples from a larger cohort of patients with

breast cancer. These projects have the potential to identify blood biomarkers

for early breast cancer improving the specificity of mammography, allowing

patients to be selected for auxiliary imaging based on the presence of specific

biomarkers in the blood and to identify with certainty which early precursor

lesions will progress to malignancy. Also, they have the potential to be used

to identify both early breast cancer and whether the disease has metastasized

to other sites. If confirmed in a large patient cohort, the biomarkers could be

isolated and incorporated into a non-invasive test such as a lateral flow device

that could be used for the detection of patients with early and metastatic breast

cancer and to identify the sites to which the cancer has metastasized. This

would help clinicians decide which patients will benefit of adjuvant therapy. If

the original findings cannot be replicated, we will search for suitable biomarkers

in urine or saliva samples or plasma samples using 2D gel electrophoresis and

the scioDiscover platform.

Biography

Ana Pedro working as Pharmacist in Rowland’s Pharmacy, she

works in the development of test kits for circulating biomarkers

for early and advanced breast cancer to be commercialized in

community pharmacies. Also undertaken community clinical

pharmacy research work and looking forward to develop PGDs

and educational materials to pharmacists and bring overseas

pharmacists to work in UK.

anapedrolaboratories@gmail.com

Development of circulating biomarkers for early and

advanced breast cancer

Ana Pedro

2,3

, Rod Tucker

1,2

, Michael J Lind

3

and Barbara Guinn

3

1

Robert Gordon University, UK

2

Biomarkers Ltd, UK

3

University of Hull, UK

Ana Pedro et al., Biochem Mol biol J 2019, Volume:5

DOI: 10.21767/2471-8084-C1-023