# Determination of P21 upstream signaling in the toxicity of MC and DMC DNA interstrand crosslinks (Student: Melissa Rosas)

> **NIH NIH SC3** · JOHN JAY COLLEGE OF CRIMINAL JUSTICE · 2021 · $31,689

## Abstract

Summary:
The overarching goal of the parent proposal for this “research supplement to promote diversity in
health-related research” is to investigate the relationship between the structure of stereoisomeric
DNA Interstrand Crosslinks (ICLs) formed by Mitomycin C and Decarbamoylmitomycin C and the
molecular mechanisms of these drugs. Mitomycin C (MC) is an anticancer drug currently used to
treat stomach, anal and lung cancers. The stereochemical configuration at C1’’ of MC major ICL
is R (α-ICL). In contrast, Decarbamoylmitomycin C (DMC), a derivative of MC lacking the O10
carbamoyl group, generates the S stereoisomeric ICL (β-ICL). The scientific premise of the
proposed research is that ICLs constitute the molecular basis for the cytotoxic effects of
mitomycins. The central hypothesis is that differences in the local DNA structures of the α and β-
ICLs are responsible for the distinct biochemical responses triggered by MC and DMC. In
particular, contrary to MC, the DNA-adducts generated by DMC treatment (-ICL) rapidly activate
a p53-independent cell death pathway. Thus, the study MC-DMC provides an ideal model for
identifying structural features determining the cell signaling outcome in the presence or the
absence of a functioning p53 pathway. Since p53 tumor suppressor is frequently mutated in
human cancers, the need to identify drugs and pathways that induce cell death or cell cycle arrest
independently of p53 deserves substantial attention. Within the scope of the parent project, this
supplement to promote diversity in health-related research will be used to train the candidate,
Melissa Rosas, to: 1: Synthesize oligonucleotides containing α/β ICLs; 2: Transfect cells with the
α/β ICLs and extract proteins; 3: Validate upstream signaling molecules, such as ATR/BRCA1,
involved in the p21 signaling pathway triggered by the presence of either the α or β ICL. Melissa’s
long-term goal is to become a clinical pathologist. The training and activities proposed will improve
Melissa’s chances to access medical schools by fostering crucial technical and professional skills.
As Melissa gains new exposure to the research environment, she will become more comfortable
interacting with other scientists and sharing her work. This increased confidence will be an asset
during medical school interviews and presentations. In order to further enhance Melissa’s
competitiveness to access medical programs, she will present her research findings at
conferences and publish at least one manuscript. She will also receive career advisement from
Dr Edgardo Sanabria-Valentin, the PRISM Associate Program Director. As the Pre-Health Career
Advisor, he will assist Melissa in considering long-term career goals and the skills needed to
achieve them as well as in preparing her medical school application material.

## Key facts

- **NIH application ID:** 10377882
- **Project number:** 3SC3GM105460-07S2
- **Recipient organization:** JOHN JAY COLLEGE OF CRIMINAL JUSTICE
- **Principal Investigator:** Elise Champeil
- **Activity code:** SC3 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2021
- **Award amount:** $31,689
- **Award type:** 3
- **Project period:** 2021-07-01 → 2023-03-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10377882

## Citation

> US National Institutes of Health, RePORTER application 10377882, Determination of P21 upstream signaling in the toxicity of MC and DMC DNA interstrand crosslinks (Student: Melissa Rosas) (3SC3GM105460-07S2). Retrieved via AI Analytics 2026-05-23 from https://api.ai-analytics.org/grant/nih/10377882. Licensed CC0.

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