دورية أكاديمية

Pilot and feasibility study: comparative proteomic analysis by 2-DE MALDI TOF/TOF MS reveals 14-3-3 proteins as putative biomarkers of response to neoadjuvant chemotherapy in ER-positive breast cancer

التفاصيل البيبلوغرافية
العنوان: Pilot and feasibility study: comparative proteomic analysis by 2-DE MALDI TOF/TOF MS reveals 14-3-3 proteins as putative biomarkers of response to neoadjuvant chemotherapy in ER-positive breast cancer
المؤلفون: ElFadl, Dalia, Drew, Philip J., Agarwal, Vijay, Hodgkinson, Victoria C., Cawkwell, Lynn, Lind, Michael, Fox, John N., McManus, Penelope L., Mahapatra, Tapan K., Kneeshaw, Peter J., Lind, Michael J., Agarwala, Vijay
بيانات النشر: Elsevier
سنة النشر: 2012
المجموعة: University of Hull: Repository@Hull
مصطلحات موضوعية: 14-3-3, Biomarkers, Breast cancer, Neoadjuvant chemotherapy, Mass spectrometry, Proteomics, Health and Health Inequalities
الوصف: Neoadjuvant chemotherapy is used to treat oestrogen receptor-positive breast cancer however chemo-resistance is a major obstacle in this molecular subtype. The ability to predict tumour response would allow chemotherapy administration to be directed towards patients who would most benefit, thus maximising treatment efficacy. We aimed to identify protein biomarkers associated with response to neoadjuvant chemotherapy, in a pilot study using comparative 2-DE MALDI TOF/TOF MS proteomic analysis of breast tumour samples. A total of 3 comparative proteomic experiments were performed, comparing protein expression between chemotherapy-sensitive and chemotherapy-resistant oestrogen receptor-positive invasive ductal carcinoma tissue samples. This identified a list of 132 unique proteins that were significantly differentially expressed (≥ 2 fold) in chemotherapy resistant samples, 57 of which were identified in at least two experiments. Ingenuity® Pathway Analysis was used to map the 57 DEPs onto canonical signalling pathways. We implicate several isoforms of 14-3-3 family proteins (theta/tau, gamma, epsilon, beta/alpha and zeta/delta), which have previously been associated with chemotherapy resistance in breast cancer. Extensive clinical validation is now required to fully assess the role of these proteins as putative markers of chemotherapy response in luminal breast cancer subtypes.
نوع الوثيقة: article in journal/newspaper
اللغة: unknown
تدمد: 1874-3919
العلاقة: https://hull-repository.worktribe.com/output/417648Test; Journal of proteomics; Volume 75; Issue 9; Pagination 2745-2752
DOI: 10.1016/j.jprot.2012.03.049
الإتاحة: https://doi.org/10.1016/j.jprot.2012.03.049Test
https://hull-repository.worktribe.com/output/417648Test
رقم الانضمام: edsbas.1BEEEFF3
قاعدة البيانات: BASE
الوصف
تدمد:18743919
DOI:10.1016/j.jprot.2012.03.049