Rich66
06-23-2009, 02:08 PM
Curb A Cancer's Deadliness? Potent Metastasis Inhibitor Identified
LINK (http://www.sciencedaily.com/releases/2009/06/090622171406.htm)
ScienceDaily (June 23, 2009) — Researchers at Children's Hospital Boston have isolated a potent inhibitor of tumor metastasis made by tumor cells, one that could potentially be harnessed as a cancer treatment. Their findings were published in the online Early Edition of the Proceedings of the National Academy of Sciences during the week of June 22.
Metastasis—the migration of cancer cells to other parts of the body—is one of the leading causes of death from cancer, and there is no approved therapy for inhibiting or treating metastases. Randoph S. Watnick, PhD, an assistant professor in the Vascular Biology Program at Children's, has been finding that metastatic tumors prepare landing places in distant organs for their metastases, by secreting certain proteins that encourage tumor growth and attract feeder blood vessels. Now, he and his colleagues show that non-metastatic tumors secrete a protein called prosaposin -- which inhibits metastasis by causing production of factors that block the growth of blood vessels.
Cells from localized prostate and breast tumors, which didn't metastasize, secreted high levels of prosaposin, they found, while metastatic tumors secreted very little. When the researchers injected mice with tumor cells that were known to be highly metastatic, but to which they had added prosaposin, lung metastases were reduced by 80 percent and lymph node metastases were completely eliminated, and survival time was significantly increased. Conversely, when they suppressed prosaposin expression in tumor cells, they saw more metastases.
When prosaposin was directly injected into mice that had also received an injection of tumor cells, the tumor cells formed virtually no metastases in the lung, or, if they did, formed much smaller colonies. These mice lived at least 30 percent longer than mice not receiving prosaposin.
Watnick and colleagues also demonstrated that prosaposin stimulates activity of the well-known tumor suppressor p53 in the connective tissue (stroma) surrounding the tumor. This in turn stimulated production of thrombospondin-1, a natural inhibitor of blood vessel growth (angiogenesis), both in the tumor stroma and in cells at the distant location.
"Prosaposin, or derivatives that stimulate p53 activity in a similar manner in the tumor stroma, might be an effective way to inhibit the metastatic process in humans," says Watnick.
If this bears out, Watnick envisions treating cancer patients for their primary tumor, and concurrently giving them drugs to prevent metastases or slow their growth. "While we may not be able to keep patients from getting cancer, we can potentially keep them metastasis-free," he says.
Initially, Watnick's scientific interest was focused on metastatic cancer cells; he hoped to use proteomics techniques to isolate different proteins that steered metastases to different parts of the body (explaining, for example, why lung cancer often metastasizes to bone, or prostate cancer to liver). But the late Judah Folkman, MD, founder of the Vascular Biology program at Children's, encouraged him to focus on the metastasis inhibitor -- prosaposin. "You might have a drug right here," he told Watnick.
A patent has been filed by Children's Hospital Boston on the discovery. The hospital's Technology and Innovation Development Office is in active discussions to license prosaposin for commercial development.
The study was funded by the Gackstatter Foundation, a grant from the National Aeronautics and Space Administration and a Breast Cancer Innovator Award from the Department of Defense.
Found in milk but inflammatory growth factors may outweigh pros. Whey seems safer:
Journal of Dairy Science Vol. 80 No. 2 264-272
© 1997 by American Dairy Science Association ® (http://jds.fass.org/misc/terms.shtml)<vardef id="TEXT"><!-- Page generated by HighWire's AbhwRetro system-->
Prosaposin, a Neurotrophic Factor: Presence and Properties in Milk
<nobr>Stuart Patton <sup>1</sup></nobr>, <nobr>Geoffrey S. Carson <sup>1</sup></nobr>, <nobr>Masao Hiraiwa <sup>1</sup></nobr>, <nobr>John S. O'Brien <sup>1</sup></nobr>, and <nobr>Akira Sano <sup>2</sup></nobr>
<sup>1</sup> Department of Neurosciences, 0634J, University of California San Diego, La Jolla 92093
<sup>2</sup> Department of Neuropsychiatry, Ehime University School of Medicine, Ehime 791-02, Japan
The presence of prosaposin, the precursor of the sphingolipid<sup> </sup>activator proteins (saposins A, B, C, and D), was investigated<sup> </sup>in bovine milk. The milk proteins were resolved by SDS-PAGE,<sup> </sup>blotted onto nitrocellulose sheets, and immunostained. Each<sup> </sup>of three appropriate antibodies defined a band from milk that<sup> </sup>matched in mobility the reference prosaposin from human milk<sup> </sup>at a relative molecular mass of 66,000. Evidence of mature saposins<sup> </sup>was not found. Prosaposin was detected in milk of other species<sup> </sup>(chimpanzee, rhesus, goat, and rat) and was consistently observed<sup> </sup>in samples of retail milk and from individual cows. Prosaposin<sup> </sup>was not associated with particulate matter (fat globules, casein<sup> </sup>micelles, membrane fragments, and somatic cells) in either human<sup> </sup>or bovine milk. Rather, prosaposin was located exclusively in<sup> </sup>the milk serum (whey), existing in monomeric form, as revealed<sup> </sup>by nondenaturing PAGE. A commercial whey protein concentrate<sup> </sup>(75% protein) appeared to retain milk prosaposin quantitatively.<sup> </sup>Properties that were useful in the isolation of prosaposin from<sup> </sup>milk were its binding to concanavalin A, retention by anion-exchange<sup> </sup>cellulose, and resistance to precipitation by heating. The possibility<sup> </sup>that bovine milk prosaposin nutritionally benefits the humans<sup> </sup>who consume it is enhanced by the fact that only part of its<sup> </sup>saposin C segment is required for neurotrophic activity.</vardef>
LINK (http://www.sciencedaily.com/releases/2009/06/090622171406.htm)
ScienceDaily (June 23, 2009) — Researchers at Children's Hospital Boston have isolated a potent inhibitor of tumor metastasis made by tumor cells, one that could potentially be harnessed as a cancer treatment. Their findings were published in the online Early Edition of the Proceedings of the National Academy of Sciences during the week of June 22.
Metastasis—the migration of cancer cells to other parts of the body—is one of the leading causes of death from cancer, and there is no approved therapy for inhibiting or treating metastases. Randoph S. Watnick, PhD, an assistant professor in the Vascular Biology Program at Children's, has been finding that metastatic tumors prepare landing places in distant organs for their metastases, by secreting certain proteins that encourage tumor growth and attract feeder blood vessels. Now, he and his colleagues show that non-metastatic tumors secrete a protein called prosaposin -- which inhibits metastasis by causing production of factors that block the growth of blood vessels.
Cells from localized prostate and breast tumors, which didn't metastasize, secreted high levels of prosaposin, they found, while metastatic tumors secreted very little. When the researchers injected mice with tumor cells that were known to be highly metastatic, but to which they had added prosaposin, lung metastases were reduced by 80 percent and lymph node metastases were completely eliminated, and survival time was significantly increased. Conversely, when they suppressed prosaposin expression in tumor cells, they saw more metastases.
When prosaposin was directly injected into mice that had also received an injection of tumor cells, the tumor cells formed virtually no metastases in the lung, or, if they did, formed much smaller colonies. These mice lived at least 30 percent longer than mice not receiving prosaposin.
Watnick and colleagues also demonstrated that prosaposin stimulates activity of the well-known tumor suppressor p53 in the connective tissue (stroma) surrounding the tumor. This in turn stimulated production of thrombospondin-1, a natural inhibitor of blood vessel growth (angiogenesis), both in the tumor stroma and in cells at the distant location.
"Prosaposin, or derivatives that stimulate p53 activity in a similar manner in the tumor stroma, might be an effective way to inhibit the metastatic process in humans," says Watnick.
If this bears out, Watnick envisions treating cancer patients for their primary tumor, and concurrently giving them drugs to prevent metastases or slow their growth. "While we may not be able to keep patients from getting cancer, we can potentially keep them metastasis-free," he says.
Initially, Watnick's scientific interest was focused on metastatic cancer cells; he hoped to use proteomics techniques to isolate different proteins that steered metastases to different parts of the body (explaining, for example, why lung cancer often metastasizes to bone, or prostate cancer to liver). But the late Judah Folkman, MD, founder of the Vascular Biology program at Children's, encouraged him to focus on the metastasis inhibitor -- prosaposin. "You might have a drug right here," he told Watnick.
A patent has been filed by Children's Hospital Boston on the discovery. The hospital's Technology and Innovation Development Office is in active discussions to license prosaposin for commercial development.
The study was funded by the Gackstatter Foundation, a grant from the National Aeronautics and Space Administration and a Breast Cancer Innovator Award from the Department of Defense.
Found in milk but inflammatory growth factors may outweigh pros. Whey seems safer:
Journal of Dairy Science Vol. 80 No. 2 264-272
© 1997 by American Dairy Science Association ® (http://jds.fass.org/misc/terms.shtml)<vardef id="TEXT"><!-- Page generated by HighWire's AbhwRetro system-->
Prosaposin, a Neurotrophic Factor: Presence and Properties in Milk
<nobr>Stuart Patton <sup>1</sup></nobr>, <nobr>Geoffrey S. Carson <sup>1</sup></nobr>, <nobr>Masao Hiraiwa <sup>1</sup></nobr>, <nobr>John S. O'Brien <sup>1</sup></nobr>, and <nobr>Akira Sano <sup>2</sup></nobr>
<sup>1</sup> Department of Neurosciences, 0634J, University of California San Diego, La Jolla 92093
<sup>2</sup> Department of Neuropsychiatry, Ehime University School of Medicine, Ehime 791-02, Japan
The presence of prosaposin, the precursor of the sphingolipid<sup> </sup>activator proteins (saposins A, B, C, and D), was investigated<sup> </sup>in bovine milk. The milk proteins were resolved by SDS-PAGE,<sup> </sup>blotted onto nitrocellulose sheets, and immunostained. Each<sup> </sup>of three appropriate antibodies defined a band from milk that<sup> </sup>matched in mobility the reference prosaposin from human milk<sup> </sup>at a relative molecular mass of 66,000. Evidence of mature saposins<sup> </sup>was not found. Prosaposin was detected in milk of other species<sup> </sup>(chimpanzee, rhesus, goat, and rat) and was consistently observed<sup> </sup>in samples of retail milk and from individual cows. Prosaposin<sup> </sup>was not associated with particulate matter (fat globules, casein<sup> </sup>micelles, membrane fragments, and somatic cells) in either human<sup> </sup>or bovine milk. Rather, prosaposin was located exclusively in<sup> </sup>the milk serum (whey), existing in monomeric form, as revealed<sup> </sup>by nondenaturing PAGE. A commercial whey protein concentrate<sup> </sup>(75% protein) appeared to retain milk prosaposin quantitatively.<sup> </sup>Properties that were useful in the isolation of prosaposin from<sup> </sup>milk were its binding to concanavalin A, retention by anion-exchange<sup> </sup>cellulose, and resistance to precipitation by heating. The possibility<sup> </sup>that bovine milk prosaposin nutritionally benefits the humans<sup> </sup>who consume it is enhanced by the fact that only part of its<sup> </sup>saposin C segment is required for neurotrophic activity.</vardef>