Abstract C118: AI/ML-assisted detection of HMGA2 RNA isoforms in prostate cancer patient tissue

Abstract RNA In Situ Hybridization (RISH) is a powerful tool to analyze RNA expression spatially within cells and tissues. However, tools to quantify this technology is not readily available due to high cost of the software available to under-resourced communities. We therefore partnered with the Center for Equitable Artificial Intelligence and Machine Learning Systems (CEAMLS) to identify and quantify HMGA2, a biomarker associated with cancer metastasis and resistance to therapy. RISH was utilized to examine the RNA expression of HMGA2 full-length (wild-type) and HMGA2 truncated in prostate cancer (PCa) tissue from 81 patients. Artificial Intelligence and Machine Learning (AI/ML) was utilized to train a sample data set before analyzing the entire cohort. RISH demonstrated that HMGA2 wild-type isoform was more abundant and increased with Gleason grade in tissues from men of African descent compared to their European American and Asian counterparts. However, HMGA2 truncated isoform presented no clear pattern and was less abundant. Our research suggests that AI/ML may be feasible methods to analyze RISH data. Additionally, HMGA2 wild-type may be a biomarker associated with PCa disparities. This study underscores the necessity for collaboration between basic and clinical scientists in using AI/ML to better understand biomarkers in cancer progression and disparities. Acknowledgements: The authors acknowledge the use of core facilities supported by the National Institute on Minority Health and Health Disparities through grant number 5U54MD013376 and National Institute of General Medical Sciences through grant number 5UL1GM118973 Citation Format: Bor-Jang Hwang, Oluwatunmise Akinniyi, Sharon Harrison, Dennise Gibbs, Charles G. Waihenya, Andrew Gachii, Precious E. Dike, Camille Ragin, Fahmi Khalifi, Valerie Odero-Marah. AI/ML-assisted detection of HMGA2 RNA isoforms in prostate cancer patient tissue [abstract]. In: Proceedings of the 18th AACR Conference on the Science of Cancer Health Disparities; 2025 Sep 18-21; Baltimore, MD. Philadelphia (PA): AACR; Cancer Epidemiol Biomarkers Prev 2025;34(9 Suppl):Abstract nr C118.

Authors

Institutions

Publication Details

Journal
Cancer Epidemiology Biomarkers & Prevention
Published
2025-09-18
DOI
https://doi.org/10.1158/1538-7755.disp25-c118
Primary Topic
Prostate Cancer Treatment and Research
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Abstract C118: AI/ML-assisted detection of HMGA2 RNA isoforms in prostate cancer patient tissue

Oluwatunmise Akinniyi, Precious Elechi Dike, Camille Ragin, Sharon Harrison et al.
Cancer Epidemiology Biomarkers & Prevention
Prostate Cancer Treatment and Research
article

Abstract C118: AI/ML-assisted detection of HMGA2 RNA isoforms in prostate cancer patient tissue

Oluwatunmise Akinniyi, Precious Elechi Dike, Camille Ragin, Sharon Harrison, Charles G. Waihenya, Denise Gibbs, Andrew Gachii, Bor-Jang Hwang, Valerie Odero‐Marah, Fahmi Khalifi
article en

Abstract

Abstract RNA In Situ Hybridization (RISH) is a powerful tool to analyze RNA expression spatially within cells and tissues. However, tools to quantify this technology is not readily available due to high cost of the software available to under-resourced communities. We therefore partnered with the Center for Equitable Artificial Intelligence and Machine Learning Systems (CEAMLS) to identify and quantify HMGA2, a biomarker associated with cancer metastasis and resistance to therapy. RISH was utilized to examine the RNA expression of HMGA2 full-length (wild-type) and HMGA2 truncated in prostate cancer (PCa) tissue from 81 patients. Artificial Intelligence and Machine Learning (AI/ML) was utilized to train a sample data set before analyzing the entire cohort. RISH demonstrated that HMGA2 wild-type isoform was more abundant and increased with Gleason grade in tissues from men of African descent compared to their European American and Asian counterparts. However, HMGA2 truncated isoform presented no clear pattern and was less abundant. Our research suggests that AI/ML may be feasible methods to analyze RISH data. Additionally, HMGA2 wild-type may be a biomarker associated with PCa disparities. This study underscores the necessity for collaboration between basic and clinical scientists in using AI/ML to better understand biomarkers in cancer progression and disparities. Acknowledgements: The authors acknowledge the use of core facilities supported by the National Institute on Minority Health and Health Disparities through grant number 5U54MD013376 and National Institute of General Medical Sciences through grant number 5UL1GM118973 Citation Format: Bor-Jang Hwang, Oluwatunmise Akinniyi, Sharon Harrison, Dennise Gibbs, Charles G. Waihenya, Andrew Gachii, Precious E. Dike, Camille Ragin, Fahmi Khalifi, Valerie Odero-Marah. AI/ML-assisted detection of HMGA2 RNA isoforms in prostate cancer patient tissue [abstract]. In: Proceedings of the 18th AACR Conference on the Science of Cancer Health Disparities; 2025 Sep 18-21; Baltimore, MD. Philadelphia (PA): AACR; Cancer Epidemiol Biomarkers Prev 2025;34(9 Suppl):Abstract nr C118.

Cancer Epidemiology Biomarkers & PreventionVol. 34(9_Supplement)
University of Nairobi (KE), Fox Chase Cancer Center (US), Morgan State University (US)
Openalex Percentile: Top 63%
Prostate Cancer Treatment and Research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.