A novel enzyme that may play a major role in the progression or metastasis of cancer cells has been identified by scientists at the University of California, San Diego.
The have discovered a previously unknown kinase that regulates cell proliferation, shape and migration.
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According to researchers, the discovery could provide new target for future anticancer therapies.
Richard L. Klemke, professor of pathology at the UCSD School of Medicine and the Moores Cancer Center, and colleagues say the new kinase or enzyme regulates the cytoskeleton - the internal framework of tiny filaments and microtubules in cells that gives them shape, coherence and the ability to move.
![Cervical Cancer - Incidence]( "Cervical Cancer - Incidence")
Cervical cancer is the second most common cancer among women and is the primary cause of cancer-related deaths in developing countries
"This molecule may be an important new target for future anticancer therapies and a clinical biomarker that predicts whether a cancer is likely to spread," said Klemke.
Proper regulation of the cytoskeleton is important to many fundamental cellular functions, including axon/dendrite formation, migration, differentiation and proliferation.
Conversely, deregulation of the cytoskeleton can contribute to a variety of human diseases, including cancer metastasis or the spread of tumors to other parts of the body.
The new kinase - called pseudopodium-enriched atypical kinase one or PEAK1 - plays a central role in the formation of cellular pseudopodia.
Greek for "false foot," a pseudopodium is a highly specialized structure that protrudes from the surface of migrating cells.
It attaches the leading, extending membrane of the cell to its underlying substrate, and then helps pull the cell forward. By endlessly repeating this process, a cell is able to move in a productive manner.
Jonathan A. Kelber, leading author on the paper and postdoctoral fellow in Klemke's lab, said: "Cancer cells capitalize on their innate ability to move in this fashion when they metastasise. Cancer cells detach from the primary tumour, invade the extracellular milieu and then enter the vascular system from which they can spread and seed new tumours in distant tissues."
Discovering PEAK1 provides researchers with a new player to study and investigate, one that may have significant influence in the biology of cells, particularly cancer cells.
Evidence from mouse studies suggests PEAK1 is an important player during tumour growth, and Klemke's team has further demonstrated that PEAK1 levels are increased in primary and metastatic samples from human colon cancer patients. Whether PEAK1 is capable of transforming non-tumour cells into cancer cells remains to be determined.
"One exciting fact is that PEAK1 has kinase activity, which suggests you can design a small molecule drug that would specifically inhibit its activity. But that work lies in the future. First, we need to fully identify the role of its kinase domain in tumor progression," said Kelber.
The research has been published in the May 31 online Early Edition of the Proceedings of the National Academy of Sciences.
Source: ANI
Cervical Cancer - Incidence
Cervical cancer is the second most common cancer among women and is the primary cause of cancer-related deaths in developing countries
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"This molecule may be an important new target for future anticancer therapies and a clinical biomarker that predicts whether a cancer is likely to spread," said Klemke.
Proper regulation of the cytoskeleton is important to many fundamental cellular functions, including axon/dendrite formation, migration, differentiation and proliferation.
Conversely, deregulation of the cytoskeleton can contribute to a variety of human diseases, including cancer metastasis or the spread of tumors to other parts of the body.
The new kinase - called pseudopodium-enriched atypical kinase one or PEAK1 - plays a central role in the formation of cellular pseudopodia.
Greek for "false foot," a pseudopodium is a highly specialized structure that protrudes from the surface of migrating cells.
It attaches the leading, extending membrane of the cell to its underlying substrate, and then helps pull the cell forward. By endlessly repeating this process, a cell is able to move in a productive manner.
Jonathan A. Kelber, leading author on the paper and postdoctoral fellow in Klemke's lab, said: "Cancer cells capitalize on their innate ability to move in this fashion when they metastasise. Cancer cells detach from the primary tumour, invade the extracellular milieu and then enter the vascular system from which they can spread and seed new tumours in distant tissues."
Discovering PEAK1 provides researchers with a new player to study and investigate, one that may have significant influence in the biology of cells, particularly cancer cells.
Evidence from mouse studies suggests PEAK1 is an important player during tumour growth, and Klemke's team has further demonstrated that PEAK1 levels are increased in primary and metastatic samples from human colon cancer patients. Whether PEAK1 is capable of transforming non-tumour cells into cancer cells remains to be determined.
"One exciting fact is that PEAK1 has kinase activity, which suggests you can design a small molecule drug that would specifically inhibit its activity. But that work lies in the future. First, we need to fully identify the role of its kinase domain in tumor progression," said Kelber.
The research has been published in the May 31 online Early Edition of the Proceedings of the National Academy of Sciences.
Source: ANI
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