Work by scientists in The Netherlands has contradicted the notion that breast cancer metastases behave differently to their primary tumors.
PhD student Britta Weigelt told the meeting of the 4th European Breast Cancer Conference that, contrary to what had been thought previously, any primary breast cancer cell was capable of producing secondary cancer cells, which then spread to other parts of the body. These secondary cancer cells had a strikingly similar genetic make-up to their parent cells and behaved in a similar way. Therefore, metastases were likely to have the same response to a particular treatment as their primary tumor.
The discovery has implications for the treatment of breast cancer once researchers have identified the ways that genetically different tumors respond to a variety of therapies. Based on the genetic profile of a patient's tumor, doctors could choose the best treatment for that particular type of tumor (from specific types of chemo-, radio- or hormonal therapies) and treat the patient with it from the time of diagnosis.
Such early (neo-adjuvant) treatment could not only shrink the primary tumor but might also prevent the outgrowth of micrometastases, thereby saving lives, as metastases that occur in other parts of the body can be difficult to treat successfully and are the main cause of death in breast cancer.
Weigelt said: "Until now it was largely unknown whether the characteristics of breast cancer that define the growth rate and therapy response of the primary tumor were alike in the metastases. Furthermore, it was unclear whether all primary breast cancer cells were capable of metastasizing, or only some of them."
In the first study to do this, Weigelt and her colleagues at the Netherlands Cancer Institute in Amsterdam compared the activities of genes in samples of primary breast tumors from 15 patients with their matching lymph node metastases, and also compared primary tumors with matching metastases that had spread to more distant parts of the body in another eight patients.
"We showed, by gene-expression profiling, that human primary breast tumors are strikingly similar to their regional lymph node metastases, as well as to more distant metastases in the same patient," said Weigelt.
"The study adds additional pieces in the puzzle of how the metastatic process in breast cancer might work. Furthermore, we showed that the metastatic outgrowths at distant organs did not result in major changes in gene expression, as had been postulated previously.
"Now, we plan to investigate more precisely when breast tumors acquire their ability to metastasize and the associated genetic causes. This could enable us to predict which tumors are more likely to metastasize so that they could be treated appropriately to prevent this happening."
SOURCE:
4th European Breast Cancer Conference, March 18, 2004, Hamburg, Germany