# Role of extracellular matrix malleability in mediating breast cancer cell invasion and migration

> **NIH NIH R37** · STANFORD UNIVERSITY · 2022 · $360,428

## Abstract

Ductal carcinoma is the most common form of breast cancer and progresses to Invasive Ductal Carcinoma
(IDC) when the carcinoma invades through the basement membrane (BM) into the stromal tissue. Invasion is a
key step in ductal carcinoma progression that is associated with an increased likelihood for metastasis, the
most deadly aspect of breast cancer. During metastasis, cancer cells must also invade BM during intravasation
and extravasation. Cancer cells are thought to utilize proteases to degrade the BM during invasion of the BM
using specialized structures known as invadopodia. Known modes of protease-independent invasion and
migration, involving cells squeezing through pores in the ECM, would be inhibited by the nanoporous nature of
the BM. However, physiological ECM is viscoelastic, exhibiting some characteristics of viscous fluids, and
cellular forces can induce flow and permanent deformation of the matrix. In other words, viscoelastic ECM is
malleable, and cell generated forces may expand pores, providing a mechanism for cells to mechanically
remodel the ECM and physically clear a path for migration, independent of proteases. While malleability is
related to matrix viscosity, it is distinct from matrix elasticity. Interestingly, malignant breast lesions have been
found to exhibit a greater degree of viscosity than benign lesions. Importantly, the concept of malleability might
be relevant to protease-dependent migration as well, as the action of proteases may be to make the matrix
more malleable. The specific hypothesis to be tested in this application is that malleability is a key physical
parameter of the BM that mediates protease-dependent and protease-independent cancer cell invasion and
migration. This hypothesis is supported by preliminary studies finding that cancer cells can invade and migrate
through nanoporous matrices that contain BM ligands with intermediate or high-malleability in a protease-
independent manner, utilizing invadopodial like protrusions to initiate invasion, but are unable to invade and
migrate through matrices with low malleability. This hypothesis will be tested by pursuing the following three
specific aims: (1) Fabricate materials for 3D cell culture with independently tunable malleability that present
ligands and stiffness relevant to the BM of mammary epithelium; (2) Determine how ECM malleability regulates
invadopodial protrusions; and (3)! Identify molecular and biophysical mechanisms underlying protease-
independent migration through ECMs with different levels of malleability. This approach is innovative because
of its focus on understanding the role of malleability in mediating protease-independent and -dependent
invasion and migration, as malleability is a physical characteristic of ECM, related to matrix viscosity but
distinct from elasticity or density, which has been largely ignored in studies to date. The proposed research is
significant because it will reveal the role of ECM malleability in mediati...

## Key facts

- **NIH application ID:** 10314031
- **Project number:** 5R37CA214136-05
- **Recipient organization:** STANFORD UNIVERSITY
- **Principal Investigator:** Ovijit Chaudhuri
- **Activity code:** R37 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2022
- **Award amount:** $360,428
- **Award type:** 5
- **Project period:** 2018-01-01 → 2022-12-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10314031

## Citation

> US National Institutes of Health, RePORTER application 10314031, Role of extracellular matrix malleability in mediating breast cancer cell invasion and migration (5R37CA214136-05). Retrieved via AI Analytics 2026-05-21 from https://api.ai-analytics.org/grant/nih/10314031. Licensed CC0.

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