User:Melissa Wong

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{{Template:OHSU Knight Cancer Institute Research Groups}}
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==Contact Info==
==Contact Info==
[[Image:OWWEmblem.png|thumb|right|Melissa Wong (an artistic interpretation)]]
[[Image:MissyWong'sLab.jpg|thumb|right|Wong Lab]]
*Melissa Wong
*Melissa Wong

Current revision

Equipped with his five senses, man explores the universe around him and calls the adventure Science.  ~Edwin Powell Hubble, The Nature of Science, 1954

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Contact Info

Wong Lab
Wong Lab
  • 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.


  • Year, PhD, Institute
  • Year, MS, Institute
  • Year, BS, Institute

Research interests

  1. Interest 1
  2. Interest 2
  3. Interest 3


Error fetching PMID 6947258:
Error fetching PMID 13718526:
  1. Error fetching PMID 6947258: [Paper1]
  2. Error fetching PMID 13718526: [Paper2]
    leave a comment about a paper here

  3. Mark Ptashne. A genetic switch. Cold Spring Harbor, N.Y.: Cold Spring Harbor Laboratory Press, 2004. isbn:0879697164. [Book1]
All Medline abstracts: PubMed HubMed

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