User:Melissa Wong: Difference between revisions
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==Contact Info== | ==Contact Info== | ||
[[Image:OWWEmblem.png|thumb|right|Melissa Wong (an artistic interpretation)]] | [[Image:OWWEmblem.png|thumb|right|Melissa Wong (an artistic interpretation)]] | ||
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*[[Special:Emailuser/Melissa Wong|Email me through OpenWetWare]] | *[[Special:Emailuser/Melissa Wong|Email me through OpenWetWare]] | ||
==Wong Laboratory== | |||
:Project Summaries | |||
;The implication of circulating bone marrow-derived stem cells and cell fusion on intestinal tissue regeneration and tumorigenesis | |||
Our laboratory has shown that circulating BMDCs fuse with intestinal stem cells upon tissue injury, inclusive of intestinal inflammatory disease and intestinal carcinogenesis. We now extend these studies to identify the cellular mediators of fusion, the underlying mechanism, and the long-term fate to the cell fusion hybrids. Our studies offer an exciting alternative view of how tissue regenerates and have the potential to explain how chronic injury can lead to intestinal tumorigenesis. | |||
;Role of Wnt signaling in regulating the intestinal stem cell niche | |||
Temporal manipulation of the Wnt/β-catenin mediated signaling pathway using genetically engineered mice and of the non-canonical Wnt signaling pathway using lentiviral mediated delivery will facilitate an understanding of how the intestinal stem cell niche is regulated during development and disease. | |||
;Identification of markers for intestinal stem cells and intestinal cancer stem cells | |||
The cancer stem cell theory for why many cancers recur after treatment presents a novel target for cancer therapeutics. However, the notion that cancer stem cells arise from mutations in tissue stem cells suggests that these two cell populations may share similar features and targetable epitopes. We have taken a systematic approach to defining surface antigens on these two populations by generating novel monoclonal antibodies. Our studies will establish a link between these two populations and may provide novel epitopes that are unique to the cancer stem cell that can be used for targeted therapy. | |||
==Education== | ==Education== |
Revision as of 13:46, 2 April 2009
Contact Info
- Melissa Wong
- Oregon Health and Science University
- Department of Dermatology
- Mailcode L468R
- 3181 SW Sam Jackson Park Rd
- Portland, OR 97239
- Email me through OpenWetWare
Wong Laboratory
- Project Summaries
- The implication of circulating bone marrow-derived stem cells and cell fusion on intestinal tissue regeneration and tumorigenesis
Our laboratory has shown that circulating BMDCs fuse with intestinal stem cells upon tissue injury, inclusive of intestinal inflammatory disease and intestinal carcinogenesis. We now extend these studies to identify the cellular mediators of fusion, the underlying mechanism, and the long-term fate to the cell fusion hybrids. Our studies offer an exciting alternative view of how tissue regenerates and have the potential to explain how chronic injury can lead to intestinal tumorigenesis.
- Role of Wnt signaling in regulating the intestinal stem cell niche
Temporal manipulation of the Wnt/β-catenin mediated signaling pathway using genetically engineered mice and of the non-canonical Wnt signaling pathway using lentiviral mediated delivery will facilitate an understanding of how the intestinal stem cell niche is regulated during development and disease.
- Identification of markers for intestinal stem cells and intestinal cancer stem cells
The cancer stem cell theory for why many cancers recur after treatment presents a novel target for cancer therapeutics. However, the notion that cancer stem cells arise from mutations in tissue stem cells suggests that these two cell populations may share similar features and targetable epitopes. We have taken a systematic approach to defining surface antigens on these two populations by generating novel monoclonal antibodies. Our studies will establish a link between these two populations and may provide novel epitopes that are unique to the cancer stem cell that can be used for targeted therapy.
Education
- Year, PhD, Institute
- Year, MS, Institute
- Year, BS, Institute
Research interests
- Interest 1
- Interest 2
- Interest 3
Publications
- Goldbeter A and Koshland DE Jr. An amplified sensitivity arising from covalent modification in biological systems. Proc Natl Acad Sci U S A. 1981 Nov;78(11):6840-4. DOI:10.1073/pnas.78.11.6840 |
- JACOB F and MONOD J. Genetic regulatory mechanisms in the synthesis of proteins. J Mol Biol. 1961 Jun;3:318-56. DOI:10.1016/s0022-2836(61)80072-7 |
leave a comment about a paper here
- ISBN:0879697164