University of Edinburgh Featured PhD Programmes
University of Leeds Featured PhD Programmes
University of Glasgow Featured PhD Programmes

Telomere length elongation following treatment with chemotherapeutic drugs. Aim: To investigate the mechanisms which leads to telomere length elongation after treatment with tricostatin A and azacytidine.


Biosciences

This project is no longer listed on FindAPhD.com and may not be available.

Click here to search FindAPhD.com for PhD studentship opportunities
Dr T Roberts Applications accepted all year round Self-Funded PhD Students Only

About the Project

Telomeres are specialised structures, which are present at the ends of chromosomes and serve to protect the chromosome from degradation during cell division. Telomeres consist of a simple repeat sequence TTAGGG, which extends for up to 15kb in young normal human somatic cells, and are associated with a set of telomeric binding proteins collectively known as shelterin. During malignant transformation of normal cells, telomeres are maintained, although often still critically short, by the activation of the enzyme telomerase or rarely by the induction of the ALT (alternative lengthening of telomeres) recombinational telomere maintenance mechanism.
Our previous studies has shown that the chemotherapeutic drugs azacytidine and tricostatin A induce telomere length elongation in breast cancer cell lines [1, 2]. As mentioned above, telomere length increase is known to occur via two main processes, telomerase upregulation and/ or Alternative Lengthening of Telomeres (ALT). The objectives of this project will be to investigate which mechanism is responsible for the elongation observed after treatment and what affects this has on the biology of the cancer cells.
A range of molecular biology techniques will be used to carry out this investigation. This will include cell culturing, RNA, DNA, protein isolation, telomere length analysis using QFISH and qPCR, TRAP assay, C-Circle analysis. The MTT assay will be used to monitor drug sensitivity/resistance following exposure to azacytidine and tricostatin A.

Funding Notes

Brunel offers a number of funding options to research students that help cover the cost of their tuition fees, contribute to living expenses or both. See more information here: https://www.brunel.ac.uk/research/Research-degrees/Research-degree-funding
Recently the UK Government made available the Doctoral Student Loans of up to £25,000 for UK and EU students and there is some funding available through the Research Councils. Many of our international students benefit from funding provided by their governments or employers. Brunel alumni enjoy tuition fee discounts of 15%.

References

1. Motevalli A, Yasaei H., Virmouni SA., Slijepcevic P., Roberts T. The effect of chemotherapeutic agents on telomere length maintenance in breast cancer cell lines. Breast Cancer Research and Treatment (2014) May 145(3) 581-591.

2. Motevalli A., Yasaei H., Virmouni A., Slijepcevic P., Mirabdulhagh, M., Roberts T. Telomere elongation in the breast cancer cell line 21NT after treatment with an epigenetic modifying drug. Journal of Cancer Therapy (2016). 7;700-711.



FindAPhD. Copyright 2005-2021
All rights reserved.