# Hypoxia-derived molecular MSI signatures to predict breast cancer outcome

> **NIH NIH R01** · JOHNS HOPKINS UNIVERSITY · 2020 · $112,585

## Abstract

We are applying for an administrative diversity supplement at the National Cancer Institute (NCI) that would
allow the talented physician-scientist Dr. Adelaja to receive additional research training within the NIH-funded
parent project R01 CA213492 (contact PI: Dr. Glunde) entitled entitled “Hypoxia-derived molecular MSI
signatures to predict breast cancer outcome”. Dr. Adelaja is eligible for the NCI diversity supplement PAR-18-
906 because he is a U.S. citizen and Black or African American. He is a clinically trained, board-certified
pathologist who came to the Johns Hopkins School of Medicine for additional research training in 2018, right
after his residency and board certification at the University of Illinois Hospital & Health Science System. The
T32 training grant on which Dr. Adelaja has been funded for the past 20 months of his postdoctoral fellowship
at Johns Hopkins is ending in a few months. Therefore, we are herewith applying for an NCI diversity
supplement for Dr. Adelaja to receive necessary additional research training to achieve his career goal of
becoming a successful physician-scientist. We have put together a compelling personalized research,
mentoring and career development plan for Dr. Adelaja's next two years of postdoctoral research training in Dr.
Glunde's lab. Currently, Dr. Adelaja is already heavily involved in Aim 3 of the parent R01 CA213492, in which
he has annotated tissue microarrays of primary and metastatic breast cancer from 17 patients and aided in
data analysis. We also proposed two additional Aims directly supporting Aim 1 of the parent R01. Dr. Adelaja
will be the lead investigator of these two new Aims, in which he will optimize an alternative fixative that will
allow for clinically relevant metabolite and lipid MALDI imaging as well as high quality histology at the same
time. Current applications typically use either fresh-frozen tissues that are optimal for metabolite and lipid
imaging but compromise the quality of histology, or formalin fixation, which is optimal for histology but
compromises the quality of metabolite and lipid MALDI imaging. In addition to the opportunity of leading a well-
defined research project, he will also take two courses to close the last remaining gaps in his training in
analytical chemistry and MALDI mass spectrometry data analysis. Dr. Adelaja will be mentored by an
experienced mentoring team. Dr. Glunde, the PI of the parent R01 and a biochemist by training, will act as his
main research mentor. Dr. Glunde's will be supported by pathology mentors Drs. Lotan and Eberhart. Drs.
Lotan, Eberhart, and Glunde will closely work with Dr. Adelaja to help him achieve his goal of becoming a
successful independent physician-scientist. They will support him in developing, writing, and submitting several
career development award applications as early-state principal investigator. The proposed training plan will
provide Dr. Adelaja with the necessary career skills of (i) improving his th...

## Key facts

- **NIH application ID:** 10137650
- **Project number:** 3R01CA213492-04S1
- **Recipient organization:** JOHNS HOPKINS UNIVERSITY
- **Principal Investigator:** Kristine Glunde
- **Activity code:** R01 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2020
- **Award amount:** $112,585
- **Award type:** 3
- **Project period:** 2017-08-15 → 2022-07-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10137650

## Citation

> US National Institutes of Health, RePORTER application 10137650, Hypoxia-derived molecular MSI signatures to predict breast cancer outcome (3R01CA213492-04S1). Retrieved via AI Analytics 2026-05-24 from https://api.ai-analytics.org/grant/nih/10137650. Licensed CC0.

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