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Printable Handouts
Navigable Slide Index
- Introduction
- Metastasis occur by a variety of mechanisms
- What is the metastatic phenotype?
- Lethal giant larvae and brain tumor
- LGL and distribution of BRAT, PROSPERO
- Neuroblast development
- Transplantation of tumor tissue
- Mutant brain cells proliferate in abdominal cavity
- Tumor cells are marked with a reporter gene
- Tumor cells from lgl or brat mutants are invasive
- There are no gaps in the epithelial sheath
- Detection of tumor cells beyond epithelial sheaths
- Tumor proliferation time and micro-metastases
- lgl and brat tumor cells are not equivalent
- Neuronal and glial markers expression
- Micro-metastases derived from the mutants
- Matrix metalloproteases are involved in metastasis
- Drosophila's MMPs and TIMP
- MMP1 accumulation
- Loss of mmp1 and tumor growth
- Loss of mmp1 and metastasis of lgl / brat tumors
- mammals tumor can stimulate host cells MMP
- brat tumors and host ovaries mmp1 transcript
- The consequence of inhibiting MMP activity
- Expression of GFP in host ovary
- Reduced MMP activity in host ovaries
- Tumor cells use MMP1 for metastasis
- utilization MMP by lgl tumor cell
- utilization MMP by brat tumor cell
- Metastasis occur by a variety of mechanisms (2)
- Acknowledgements
Topics Covered
- Recessive lethal mutations of Drosophila cause brain tumors that are metastatic
- Despite their apparent similarities, tumors caused by different mutations have different metastatic properties
- The metastasis of tumors caused by lgl mutations is enhanced by secretion of MMP1 from the tumor cells themselves
- The metastasis of tumors caused by brat mutations is not enhanced by secretion of MMP1 from the tumor cells themselves, but is enhanced by MMP1 that host cells are induced to secrete
Talk Citation
Shearn, A. (2017, September 25). Metastasis of Drosophila tumors [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved November 23, 2024, from https://doi.org/10.69645/TQRW7472.Export Citation (RIS)
Publication History
Financial Disclosures
- Prof. Allen Shearn has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.
A selection of talks on Oncology
Transcript
Please wait while the transcript is being prepared...
0:00
Hi, I'm Allen Shearn,
an emeritus Professor of Biology
at Johns Hopkins University.
The work on the "Metastasis of Drosophila
Tumors" that I'm about to describe,
was done by a talented group of graduate
students, postdoctoral fellows and
research associates.
The pioneering work in this field
was done by Elizabeth Gateff.
She began this work in the 1960s
as a graduate student at
Case-Western Reserve University
with Howard Schneiderman and
continued this work at the University of
Mainz until she retired a few years ago.
0:36
As with so
many other developmental processes,
Drosophila can be used as a model
system to study tumor metastasis.
Actually, Drosophila provided the first
example of a tumor suppressor gene.
In the 1960s Elizabeth Gateff
showed that recessive lethal
giant larvae mutations caused
neoplastic brain tumors, and
that those tumors when transplanted
into normal hosts, kill such hosts.
The evidence presented here demonstrates
that cells from such tumors
invade host tissues and
form micrometastases.
We compared the metastatic property
of cells from brain tumors caused by
mutations in two different genes.
Much to our surprise, we found that these
properties were distinctly different.
This lead us to conclude that metastasis
can be caused by a variety of mechanisms.
1:31
Metastasis involves the spread of tumor
cells from their site of origin and
their invasion into
tissues at distinct sites.
In vertebrates, the spread of these tumor
cells can occur via the lymph system or
through blood vessels.
Flies have an open circulatory system, so
the spread only occurs
through their lymph system.