96P - MMTV and breast cancer: Integration sites of MMTV in breast cancer patients and their potential role in cancer progression

Date 20 December 2015
Event ESMO Asia 2015 Congress
Session Poster presentation 2
Topics Basic Science
Breast Cancer
Presenter Hajra Sadia
Citation Annals of Oncology (2015) 26 (suppl_9): 16-33. 10.1093/annonc/mdv519
Authors H. Sadia, M.K. Gomez, T.B. Rahat, W. Naushad
  • Atta-ur-rahman School Of Applied Biosciences (asab), National University of Sciences & Technology (NUST), 44000 - Islamabad/PK

Abstract

Aim/Background

Detection of mouse mammary tumor virus (MMTV) in human breast cancer samples from all over the world has led to the acknowledgement of MMTV as a probable cause of breast cancer. Although its role is still debatable in humans, it is accepted as a cause for mammary tumors in mice. Reporting the presence of MMTV-like sequences in human breast cancer samples from Pakistani breast cancer patients, we also present a supposition that integration of MMTV might be, in part, responsible for breast cancer development.

Methods

After establishing presence in study samples, blood and tumor tissues, samples were processed for detection of probable integration sites of MMTV genome by employing linker-mediated polymerase chain reaction (LM-PCR) followed by sequence analysis of all possible clones.

Results

The study identified multiple (16) distinct, non-random integration sites of MMTV in human breast cancer tissues. MMTV-like sequence integrations have been found to be in or near transcription start sites, growth, DNA repair proteins and tumor suppressor genes, thus giving cells a distinct advantage for transformation and sustained survival.

Conclusions

Our data suggests that integration in the genome might give cells a distinct advantage for survival of transformed cells. Although the link is still not clear, further studies on these integration sites might reveal a link between MMTV-like sequences and human breast cancer. The resulting data lends support to the idea of a viral etiology of breast cancer. Furthermore, it also indicates anomalous behavior of MMTV-like sequences. Previous data suggests a totally random integration of MMTV in both mouse and human genome in cell lines. However, some sites were found to be repeating in different samples, thus, also supporting sequence specific bias in integration.

Clinical trial identification

Disclosure

All authors have declared no conflicts of interest.