Skip to main content
Explore URMC

Wilmot Cancer Institute Logo

menu
Glynis A. Scott, M.D.
Glynis A. Scott, M.D.

Glynis A. Scott, M.D.

Dermatology — Anatomic Pathology

Glynis A. Scott, M.D.

Dermatology — Anatomic Pathology


Locations

400 Red Creek Drive, Suite 200
Rochester, NY 14623
Get Directions

phone

Office

(585) 275-8811

print

Fax

(585) 273-1346

Credentials

Education:

MD | Albany Medical College of Union University — 1983

Post-doctoral Training & Residency:

Fellowship in Dermatopathology at Yale New Haven Hospital — 1987 - 1988
Internship in Internal Medicine at Albany Medical Center — 1983 - 1984
Residency in Anatomic Pathology at Yale New Haven Hospital — 1984 - 1987

Research

There are two major projects on going in my laboratory--the first is the investigation into signaling pathways of prostaglandins in human melanocytes and melanoma, and the second is the role of Plexin receptors in melanocyte and melanoma biology.
Melanocytes are pigment producing cells within the epidermis that are progenitor cells for a deadly cancer, melanoma. The production of melanin by melanocytes is a key function of melanocytes and provides photoprotection to the skin. Prostaglandins (PG) are lipid signaling molecules released by keratinocytes and melanocytes in response to ultraviolet irradiation. Our research focus is on defining signaling intermediates that mediate the effect of the two primary PG in the skin, PGE2 & PGF2?? on melanocyte dendrite extension, growth and pigment production. Our laboratory is also investigating the role of semaphorins and their receptors on melanocyte growth, differentiation, and progression to melanoma. Semaphorins are membrane bound and secreted proteins involved in neuronal pathfinding, that we have recently shown to be involved in melanocyte adhesion and dendrite formation. Our particular focus is on Semaphorin 7A and Semaphorin 4D, and their cognate receptors Plexin C1 and Plexin B1, which are lost during progression of melanocytes to melanoma. Integration of signaling intermediates with biologic functions such as proliferation, apoptosis and migration, allow us to dissect the function of PG and semaphorins in melanocyte, and to link signaling by specific receptors to downstream biologic targets important for skin pigmentation and melanoma progression.

Publications:

Bax MJ, Brown MD, Rothberg PG, Laughlin TS, Scott GA. "Pigmented epithelioid melanocytoma (animal-type melanoma): An institutional experience." Journal of the American Academy of Dermatology.. 2017 Aug 0; 77(2):328-332. Epub 2017 Apr 14.

Soong J, Scott GA. "Isolating Fc-Tagged SEMA4D Recombinant Protein from 293FT Cells." Methods in molecular biology.. 2017 1493:29-40.

Soh JM, Scott GA, Pavlovitz BT, Mercurio MG. "Metastatic rectal adenocarcinoma and anal squamous cell carcinoma masquerading as vulvar lymphangioma circumscriptum." Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology.. 2016 Oct 0; 36(7):876-878. Epub 2016 Sep 10.

View All Publications