Researchers Discover Molecule that Accelerates Tissue Regeneration
News Jun 12, 2015
A joint investigation including UT Southwestern Medical Center has found a molecule that may play a significant role in accelerating cell recovery following bone marrow transplants, liver disease, and colon disease.
The collaborative effort by UT Southwestern, Case Western Reserve University, and the University of Kentucky identified an enzyme named 15-PGDH that regulates tissue regeneration in multiple organs.
By blocking 15-PGDH in mice with the newly discovered molecule, SW033291, the researchers found that they can rescue damaged bone marrow, liver tissue, and colon tissue. Tissue regeneration is important to recovery from injury, disease, and certain medical treatments.
“Patients undergoing bone marrow transplants and patients with colitis may benefit from this approach,” said co-author Dr. James K. Willson, Associate Dean of Oncology Programs, Director of the Harold C. Simmons Comprehensive Cancer Center, Professor of Internal Medicine, and holder of The Lisa K. Simmons Distinguished Chair in Comprehensive Oncology. “We propose that SW033291 will be useful in accelerating recovery of bone marrow cells following a bone marrow transplant and may also be a treatment for colitis.”
Bone marrow transplants are a common treatment for leukemia patients, among others. According to the National Cancer Institute, it is estimated that during 2015 there will be 54,270 new cases of leukemia and an estimated 24,450 people will die of this disease.
The study is published in the journal Science.
Prostaglandin, a hormone-like fatty acid, is a key factor in chronic infections and cancer.
"These inhibitors increase prostaglandin levels in a variety of tissues. For this reason, they appear to help the healing process in at least the intestines, liver, and bone marrow. We are hopeful that inhibiting 15-PGDH represents a general strategy to promote tissue repair,” said co-author Dr. Joseph Ready, Professor of Biochemistry and member of the Simmons Cancer Center.
The new SW033291 molecule works by targeting a 15-PGDH-regulated pathway of bone marrow regeneration in which increased bone marrow prostaglandin drives the production of hematopoietic cytokines by CD45-positive marrow cells.
The UT Southwestern team discovered the molecule in collaboration with the University of Kentucky and long-time research collaborators at Case Western Reserve: Dr. Sanford Markowitz, Professor of Hematology and Oncology, and head of the Cancer Genetics Program there; and Dr. Stanton Gerson, Professor of Hematology and Oncology, and Director of the Case Comprehensive Cancer Center. Dr. Yongyou Zhang, a Case Western Reserve research associate, was a lead author on the study.
"It's been a pleasure to be involved in another example of a collaborative, multi-disciplinary team advancing the results of a high-throughput, chemical library screen toward a therapeutic possibility for an unmet medical need," said co-author Dr. Bruce Posner, Associate Professor of Biochemistry at UT Southwestern and member of the Simmons Cancer Center.
Animal venoms are the subject of study at research center based at the Butantan Institute in São Paulo. But in this case, the idea is not to find antidotes, but rather to use the properties of the venoms themselves to identify molecular targets of diseases and, armed with that knowledge, develop new compounds that can be used as medicines.