Scientists reverse pancreatic cancer progression in `time machine' made
of human cells

Date:
September 30, 2021
Source:
Purdue University
Summary:
What makes pancreatic cancer so deadly is its covert and quick
spread.

Now, a 'time machine' has shown a way to reverse the course of
cancer before it spreads throughout the pancreas.



FULL STORY ==========================================================================
What makes pancreatic cancer so deadly is its covert and quick
spread. Now, a "time machine" built by Purdue University engineers has
shown a way to reverse the course of cancer before it spreads throughout
the pancreas.


========================================================================== "These findings open up the possibility of designing a new gene therapy
or drug because now we can convert cancerous cells back into their normal state," said Bumsoo Han, a Purdue professor of mechanical engineering
and program leader of the Purdue Center for Cancer Research. Han has a
courtesy appointment in biomedical engineering.

The time machine that Han's lab built is a lifelike reproduction of a pancreatic structure called the acinus, which produces and secretes
digestive enzymes into the small intestine. Pancreatic cancer tends
to develop from chronic inflammation that happens when a mutation has
caused these digestive enzymes to digest the pancreas itself.

If there were a way to go back in time to reprogram the cancerous acinar
cells that produce those enzymes, then it might be possible to completely
reset the pancreas.

For the past decade, Stephen Konieczny, professor emeritus in Purdue's Department of Biological Sciences, has studied a potential reset button:
a gene called PTF1a.

"The PTF1a gene is absolutely critical for normal pancreas development. If
you lack the PTF1a gene, you don't develop a pancreas," Konieczny
said. "So, our whole idea was, if we turn the PTF1a gene back on
in a pancreatic cancer cell, what happens? Will we revert the cancer
phenotype? Indeed, that's exactly what happens." Konieczny collaborated
with Han's lab to take these findings in molecular biology studies to
the next level by testing them in a realistic model of the acinus -- the
time machine. The published study is featured on the cover of the Oct. 7
issue of Lab on a Chip, a journal by the Royal Society of Chemistry.



========================================================================== Researchers typically investigate possible pancreatic cancer treatment approaches in animal models, but it can take months for pancreatic cancer
to develop in an animal. Having a way to study cancer development and
treatment concepts in a microenvironment that is just as realistic would
save time and give researchers more control over the model.

The model that Purdue researchers developed overcomes a major challenge in accurately capturing the anatomical complexity of the acinus, a circular
cavity lined with cells.

"From an engineering perspective, creating this kind of three-dimensional cavity is not trivial. So, figuring out a way to build this cavity is
an innovation in itself," Han said.

Han's lab already had experience building a realistic model of another pancreatic structure, the duct, where cancer grows after emerging from
the acinus. The researchers took this knowledge and developed a new
technique that builds both the duct and acinus in a two-step "viscous fingering" process.

Here's how it works: The model, a postage stamp-size glass platform on
top of a microscope slide, has two interconnected chambers. Loading
a collagen solution into one chamber fills the finger-like shape of
a pancreatic duct, which bulges and then expands to create the cavity
structure of the acinus in the second chamber.



========================================================================== Dropping cancerous human cells into the acinar chamber made the model
even more realistic. Konieczny's lab engineered the PTF1a gene of a
pancreatic cancer cell line to turn on in the presence of doxycycline,
a compound commonly used in antibiotics. Once the gene was activated,
the cells started constructing the rest of the acinus in Han's model, indicating that they were no longer cancerous and had been reprogrammed.

"In this model, not only do the cancerous cells become reprogrammed,
but for the first time, we're able to show the normal three-dimensional architecture of the acinus, which looks very similar to the same
structures we see in a healthy pancreas," Konieczny said.

Han's lab is currently conducting experiments exploring a possible gene
therapy based on these findings.

This study was partially supported by grants from the National Institutes
of Health, the Walther Embedding Program in Physical Sciences in Oncology,
and the Purdue Center for Cancer Research, which is one of only seven
National Cancer Institute Basic Laboratory Cancer Centers in the nation.

========================================================================== Story Source: Materials provided by Purdue_University. Original written
by Kayla Wiles. Note: Content may be edited for style and length.


========================================================================== Journal Reference:
1. Stephanie M. Venis, Hye-ran Moon, Yi Yang, Sagar M. Utturkar,
Stephen F.

Konieczny, Bumsoo Han. Engineering of a functional pancreatic acinus
with reprogrammed cancer cells by induced PTF1a expression. Lab
on a Chip, 2021; 21 (19): 3675 DOI: 10.1039/d1lc00350j ==========================================================================

Link to news story: https://www.sciencedaily.com/releases/2021/09/210930140715.htm

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