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Predictive proteins: Elevated levels trigger metastatic progression of cancer cells

New biomarker may offer more precise and accurate prognoses of disease

University of California - San Diego

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Credit: Image courtesy of National Cancer Institute

Researchers at University of California, San Diego School of Medicine and Moores Cancer Center, with colleagues in Spain and Germany, have unraveled how elevated levels of particular proteins in cancer cells trigger hyperactivity in other proteins, fueling the growth and spread of a variety of cancers.

The findings are published in the February 26 online publication of Scientific Reports.

Specifically, the international team, led by senior author Pradipta Ghosh, MD, associate professor at UC San Diego School of Medicine, found that increased levels of expression of some members of a protein family called guanine nucleotide exchange factors (GEFs) triggered unsuspected hyperactivation of G proteins and subsequent progression or metastasis of cancer.

The discovery suggests GEFs offer a new and more precise indicator of disease state and prognosis. "We found that elevated expression of each GEF is associated with a shorter, progression-free survival in patients with metastatic colorectal cancer," said Ghosh. "The GEFs fared better as prognostic markers than two well-known markers of cancer progression and the clustering of all GEFs together improved the predictive accuracy of each individual family member."

In recent years, circulating tumor cells (CTCs), which are shed from primary tumors into the bloodstream and act as seeds for new tumors taking root in other parts of the body, have become a prognostic and predictive biomarker. The presence of CTCs are used to monitor the efficacy of therapies and detect early signs of metastasis.

But counting CTCs in the bloodstream has limited utility, said Ghosh. "Enumeration alone does not capture the particular characteristics of CTCs that are actually tumorigenic and most likely to cause additional malignancies."

Numerous efforts are underway to improve the value and precision of CTC analysis. Ghosh said the new findings are a step in that direction. First, that GEFs activate trimeric G proteins and second, that G protein signaling is involved in CTCs. G proteins are ubiquitous and essential molecular switches involved in transmitting external signals from stimuli into cells' interiors. They have been a subject of heightened scientific interest for many years.

Ghosh and colleagues found that elevated expressions of non-receptor GEFs activate Gαi proteins, fueling CTCs and ultimately impacting the disease course and survival of cancer patients.

"Our work shows the prognostic impact of elevated expressions of individual and clustered GEFs on survival and the benefit of transcriptome analysis of G protein regulatory proteins in cancer biology," said Ghosh. "The next step will be to carry this technology into the clinic where it can be directly applied to deciphering a patient's state of cancer and how best to treat."

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Co-authors of the study include Jorge Barbazan, Complexo Hospitalario Universitario de Santiago de Compostela/SERGAS, Santiago, Spain; Ying Kunkel, Hongying Li and Karen Messer, UC San Diego and Moores Cancer Center; and Ulrich Nitsche and Klaus-Peter Janssen, TU Munchen, Munich, Germany.

Funding support for this research came, in part, from the National Institutes of Health (grants R01CA160911, R01CA100768 and R01CA166293), the Burroughs Wellcome Fund, the American Cancer Society, a Translational and Clinical Research Award from Moores Cancer Center, the Spanish Ministry of Education, Culture and Sports, The German Ministry of Education and Research and the Kommission fur klinische Forschung.

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