New Insight Into Trastuzumab Resistance In Breast Cancer Via Genetic Approach

Main Category: Breast Cancer
Also Included In: Genetics
Article Date: 16 Oct 2007 - 4:00 PDT

email to a friend   printer friendly   view / write opinions   rate article

A new study provides important insight into the mechanisms involved in resistance to treatment of breast cancer patients with trastuzumab (Herceptin). The research, published by Cell Press in the October issue of the journal Cancer Cell, identifies markers that may help to identify patients who are unlikely to respond to trastuzumab treatment and provides a potential strategy for treating these patients.

Trastuzumab is an antibody used as a therapy for patients whose breast cancers produce excess amounts of the protein HER2. However, almost half of these breast cancer patients are nonresponsive to trastuzumab therapy or become resistant during treatment. To better understand the antitumor activity of trastuzumab, Dr. Rene Bernards from The Netherlands Cancer Institute and his colleagues used a large-scale genome-wide RNA interference screen to search for genes involved in trastuzumab resistance in breast cancer.

The researchers identified only the tumor suppressor PTEN as a modulator of trastuzumab sensitivity in a breast cancer cell line. Earlier findings had associated PTEN with resistance to trastuzumab-based therapy, and loss of PTEN is known to result in hyperactivation of the PI3K pathway. Abnormal activation of this cell survival signaling pathway has been identified in many primary breast cancers. Hyperactivation of the PI3K pathway also can be caused by activating mutations of the PIK3CA gene.

"This finding, along with the high frequency of PIK3CA activating mutations in breast cancer, led us to investigate whether PI3K pathway activity, as assessed by cancer-associated activating mutations (of PIK3CA) or altered levels of PTEN, was able to predict trastuzumab resistance in the clinic," explains Dr. Bernards. This combined analysis identified twice as many patients at increased risk for disease progression as would analyzing PTEN alone and proved to be statistically significant as a biomarker for prognosis after trastuzumab therapy, indicating that assessment of PTEN expression together with PIK3CA mutation is required for optimal prediction of disease progression after trastuzumab therapy for breast cancer.

"Importantly, this study also illustrates the power of in vitro RNAi screens combined with confirmation on patient samples to identify biomarkers useful for predicting treatment response in the clinic," says Dr. Bernards. "It is too early to use these biomarkers; further validation studies are required before they can be used in the clinic. Nevertheless, it is likely that these findings will lead to a better understanding of resistance mechanisms and how to circumvent them as well as more reliable identification of the most effective treatment for individual patients."

----------------------------
Article adapted by Medical News Today from original press release.
----------------------------

The researchers include Katrien Berns and Hugo M. Horlings of The Netherlands Cancer Institute in Amsterdam; Bryan T. Hennessy of The University of Texas, M.D. Anderson Cancer Center in Houston; Mandy Madiredjo, E. Marielle Hijmans, Karin Beelen and Sabine C. Linn of The Netherlands Cancer Institute in Amsterdam; Ana Maria Gonzalez-Angulo and Katherine Stemke-Hale of The University of Texas, M.D. Anderson Cancer Center in Houston; Michael Hauptmann and Roderick L. Beijersbergen of The Netherlands Cancer Institute in Amsterdam; Gordon B. Mills of The University of Texas, M.D. Anderson Cancer Center in Houston; and Marc J. van de Vijver, and René Bernards The Netherlands Cancer Institute in Amsterdam.

This work was supported by a grant from the NIH and the EU grant INTACT.

Berns et al.: "A Functional Genetic Approach Identifies the PI3K Pathway as a Major Determinant of Trastuzumab Resistance in Breast Cancer." Publishing in Cancer Cell 12, 395-402, October 2007. DOI 10.1016/j.ccr.2007.08.030 http://www.cancercell.org/

Source: Cathleen Genova
Cell Press