An enzyme called Brk - shown to be an accelerator of HER2-positive tumours - may serve as a potential drug target against virulent type of breast cancer, according to researchers at Cold Spring Harbor Laboratory.
Tumour cells in a particular subset of breast cancer patients churn out too much of a protein called ErbB2 - also often called HER2 - that drives the cells to proliferate unchecked.
Patients unlucky enough to be in this group have poorer prognoses and clinical outcomes than those who don't.
Moreover, patients with tumours that do respond usually develop resistance to these drugs.
Now, a team of scientists has found that Brk could serve as a drug target to fight ErbB2-positive tumours.
The researchers said that Brk helps these tumours become virulent and is also implicated in the process through which the tumours develop drug resistance.
"The limited success of existing therapy suggested to us that factors besides ErbB2, or proteins that collude with ErbB2, might nullify the effects of Herceptin and Lapatinib," explained CSHL Professor Senthil Muthuswamy, Ph.D., leader of the research team and cor-author of the study.
In the hunt for ErbB2's co-conspirators, Muthuswamy's team focused on Brk, which they knew to be over-produced in many other types of cancer, including two-thirds of all breast cancers.
A detailed analysis of changes that occurred in the genomes of a sample of breast cancer patients helped the group confirm that the expression of ErbB2 and Brk was directly linked.
By forcing the production of both ErbB2 and Brk within the same cell, they determined how Brk enhances ErbB2 activity and fortifies tumour cells against ErbB2-targeting drugs.
"Our results might explain why the strategy of using ErbB2 inhibitors alone to treat breast cancers has fallen short. These findings may also suggest a way to treat patients with advanced ErbB2-positive tumours and those who've developed resistance to ErbB2 inhibitors - an idea that we're eager to test," said Dr. Muthuswamy.
The study is published online August 21 ahead of print in Proceedings of the National Academy of Sciences.