# Proto‐Oncogene HRAS Transcript Level and Overall Survival in Stages II and III Colorectal Cancer

**Authors:** Donghyun Kim, Saima Sharif, Juan Antonio Raygoza Garay, Avanish S. Bhakta, Patrick M. Boland, Michael J. Cavnar, Michelle L. Churchman, Hassan Hatoum, Lyen C. Huang, Joseph Kim, Richard Kim, Robert W. Lentz, Sarbajit Mukherjee, Mary T. O'Donnell, Benjamin Quartey, Matthew J. Reilley, Robert J. Rounbehler, Bodour Salhia, Bryan P. Schneider, Carlos H. Chan

PMC · DOI: 10.1002/cam4.71114 · Cancer Medicine · 2025-07-31

## TL;DR

High levels of HRAS gene activity in colorectal cancer are linked to better survival, especially in patients with low KRAS activity and no KRAS mutations.

## Contribution

This study reveals that high HRAS transcript levels are associated with improved survival in stages II and III colorectal cancer.

## Key findings

- High HRAS transcript levels correlate with superior overall survival in stages II and III CRC.
- The survival benefit of high HRAS is most notable in right-sided CRC with low KRAS transcript levels and no KRAS mutations.

## Abstract

Mutational landscape is prognostic in colorectal cancer (CRC). Rat sarcoma (RAS) oncogenes, such as KRAS and NRAS, with driver mutations, portend poor survival outcomes, whereas pathologic mutations in HRAS are extremely rare, and their prognostic value remains uncertain.

This retrospective study analyzed the Oncology Research Information Exchange Network (ORIEN) alliance tumor RNA‐Seq data in Stages II and III CRC to investigate the association between RAS gene expression and survival outcomes.

High transcript levels of HRAS were associated with superior overall survival (OS). The high HRAS‐associated OS benefit was most pronounced in patients with right‐sided primary expressing low KRAS transcript levels in the absence of pathologic KRAS mutations.

Contrary to the notion that RAS family genes are proto‐oncogenic, this study demonstrates that high HRAS transcript levels are associated with superior OS in Stages II and III CRC. The potential of HRAS as a prognostic biomarker should be explored further.

## Linked entities

- **Genes:** HRAS (HRas proto-oncogene, GTPase) [NCBI Gene 3265], KRAS (KRAS proto-oncogene, GTPase) [NCBI Gene 3845], NRAS (NRAS proto-oncogene, GTPase) [NCBI Gene 4893]
- **Diseases:** colorectal cancer (MONDO:0005575), CRC (MONDO:0005575)

## Full-text entities

- **Genes:** NRAS (NRAS proto-oncogene, GTPase) [NCBI Gene 4893] {aka ALPS4, CMNS, N-ras, NCMS, NRAS1, NS6}, HRAS (HRas proto-oncogene, GTPase) [NCBI Gene 3265] {aka C-BAS/HAS, C-H-RAS, C-HA-RAS1, CTLO, H-RASIDX, HAMSV}, KRAS (KRAS proto-oncogene, GTPase) [NCBI Gene 3845] {aka 'C-K-RAS, C-K-RAS, CFC2, K-RAS2A, K-RAS2B, K-RAS4A}
- **Diseases:** tumor (MESH:D009369), CRC (MESH:D015179), Stages II and III (MESH:D062706)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12311480/full.md

## References

18 references — full list in the complete paper: https://tomesphere.com/paper/PMC12311480/full.md

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Source: https://tomesphere.com/paper/PMC12311480