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Printable Handouts
Navigable Slide Index
- Introduction
- Reductionist science meets cancer complexity
- Cancer hallmarks
- “Yin and Yang” of tumor-stroma interactions
- Different terms used to describe the tumor stroma
- High-throughput technologies for phenotyping the tumor stroma
- Hierarchy and heterogeneity of the tumor ecosystem
- Human evidence for the critical role of stroma in supporting tumor growth
- Heterotypic ligand-receptor signaling
- Computational tools can help find cell-cell interactions in the TMEN
- Tumor-associated extracellular matrix (ECM) is a critical component of the TME
- Patient-derived xenograft (PDX) models
- Chronical inflammation in cancer: An overhealing wound
- Stromal cell type in focus #1: Cancer-associated fibroblasts (CAFs)
- Origin of CAFs and activation through strinak signaling
- Fibroblasts elicit diverse outputs in homeostasis and disease
- CAFs diverse functions
- Subtypes of CAFs: converging and emerging classes with different functions
- CAFs can be tumor-suppressive (protective) in some context
- Stromal cell type in focus #2: Neurons
- Role of sympathetic and parasympathetic nerves in prostate cancer
- SNS adrenergic nerves activate an angio-metabolic switch
- Innervation and co-opted neuronal signaling modulate hallmarks of cancer
- Tumor-host interaction depends on endocrine signaling
- Cancer cell intrinsic mechanisms drive the formation of the immunosuppressive TME
- Summary
- Acknowledgements
- Thank you for your attention
Topics Covered
- Tumor microenvironment
- Extracellular matrix
- Cancer associated fibroblast (CAFs)
- CellChat
- Patient derived xenograft (PDX) model
- Angio-metabolic switch
Links
Series:
Categories:
Therapeutic Areas:
Talk Citation
Lu, X. (2025, February 27). Tumor-stroma interactions [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved March 3, 2025, from https://doi.org/10.69645/TSPZ2438.Export Citation (RIS)
Publication History
- Published on February 27, 2025
Financial Disclosures
- Dr. Xin Lu has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.
Other Talks in the Series: The Molecular Basis of Cancer
Transcript
Please wait while the transcript is being prepared...
0:00
Hello, everyone.
My name is Xin Lu.
I'm a Boler Associate
Professor at
the Department of
Biological Science
at the University of Notre Dame
in Indiana USA.
I'm also a full member of
the Indiana Comprehensive
Cancer Center.
Today, it is my
great pleasure to
introduce the topic of
tumor-stroma interaction to you.
0:25
Cancer has been a very important
topic in our research.
Historically,
scientists have taken
a reductionist science
method to study cancer,
which means that we take apart
the cancer tractable
components in
the cancer cells and
study them individually.
The idea is that we can deduce
the behavior of a tumor
based on the behavior
of the cancer cells.
Based on this approach,
scientists have achieved a lot.
For example, oncogenes and
tumor suppressor genes was
identified and a lot
of knowledge about
cell cycle and cell
death were identified.
Also, a lot of the
ligand-induced cell
signaling inside the cancer
cells was also discovered.
This is a great approach.
But at the same time
when we think about
real carcinoma tumors,
the solid tumors,
it's not just a bag
of cancer cells.
It's actually composed of
very complex cell types
including neoplastic
cancer cells,
and non-neoplastic
stromal cells.
For example, the fibroblasts,
endothelial cells, the immune
cells, neurons, et cetera.
We face this complex
microenvironment,
you only use the reductionist
science method anymore.
We have to consider
them as a whole
and we need to study the
tumor-stroma interactions.
We need to study the
concept of angiogenesis.
More importantly, in recent
decades, people have
discovered a lot in tumor
immunology and immunotherapy.
Today, my talk will
be mainly focused
on the non-immune part of
the stroma because there
will be a separate topic
about immune tumor
immunology later.