# Robust Predictor of Colon Cancer Risk

> **NIH NIH R42** · MORGAN AND MENDEL GENOMICS, INC. · 2022 · $968,518

## Abstract

Summary
At least 500,000 people in the United States have Lynch syndrome (LS), based on inheritance of a genetic
pathogenic variant in the mismatch repair (MMR) pathway, placing them at high-risk for colon and other
cancers. More than half of them is unaware of their diagnosis, because their family history is uninformative or
unknown. Genetic testing is important for identifying pathogenic variants in this pathway, but in a large number
of cases no pathogenic variant or a variant of uncertain significance is identified, leading to ambiguous and
unsatisfactory results. As more people are seeking testing for LS, accurate alternatives to sequencing are
needed to predict the molecular phenotypic effects of pathogenic variants in genes in the MMR pathway. Risk
classification scores based on flow variant assays (FVAs) are a new technology that can accurately identify
people with heterozygous germline pathogenic variants in these pathways. In response to treatment with
chemical agents, FVAs identify decreased nuclear localization of repair proteins and decreased
phosphorylation of damage-sensing proteins in cells that bear pathogenic variants in these genes. The
resulting test, Cancer Risk C (CR-C), is rapid, inexpensive and highly reproducible and can be performed on
circulating and cultured human blood cells, thus becoming a Next Generation, non-sequencing, standalone test
for diagnosing LS. The goal of this STTR project is to develop a, simple, rapid and inexpensive clinical test that
will accurately diagnose LS and can be implemented into clinical practice. Aim 1. Predict risk of developing
colon cancer based on CR-C test results. Aim 2. Prevalence of LS among microsatellite instability high (MSI-
H), MSI-Low and MSI-Stable subjects with colon cancer. Aim 3. Demonstrate analytical validity and
reproducibility of CR-C kits for LS diagnosis at 3 sites. This product will be sold to clinical laboratories in
collaboration with a designated good manufacturing practices facility commercial partner, initially as a
laboratory developed test and then as an FDA approved test. Several factors will drive this commercialization
into the $1B market cancer risk assessment market: 1. low entry and performance costs, 2. greater accuracy
than sequencing, and 3. application to understanding risks for colon, endometrial, gastric, ovarian, small bowel,
pancreatic, urinary tract, kidney, bile duct and brain cancers. The creation of simplified, commercial CR-C kits
will change the diagnosis of LS.

## Key facts

- **NIH application ID:** 10544646
- **Project number:** 2R42CA232867-02A1
- **Recipient organization:** MORGAN AND MENDEL GENOMICS, INC.
- **Principal Investigator:** Harry Ostrer
- **Activity code:** R42 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2022
- **Award amount:** $968,518
- **Award type:** 2
- **Project period:** 2018-09-13 → 2024-07-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10544646

## Citation

> US National Institutes of Health, RePORTER application 10544646, Robust Predictor of Colon Cancer Risk (2R42CA232867-02A1). Retrieved via AI Analytics 2026-05-23 from https://api.ai-analytics.org/grant/nih/10544646. Licensed CC0.

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