Abstract 1162: Revealing the transformative role of METTL13 in human hematopoietic stem cells and progression of pediatric leukemia

Abstract Childhood leukemia’s five year survival rate has been improving over the last 40 years, but still only reaches 86.3% relative survival in the United States according to the Surveillance, Epidemiology, and End Results (SEER) program in 2025. Aberrant post-transcriptional RNA modifications, specifically N6-methyladenosine (m6A) methylation and adenosine to inosine (A-to-I) editing have previously been shown to push malignant transformations of hematopoietic stem cells (HSC). In order to unravel the mechanism behind these RNA modifiers and decipher whether methyltransferases (METTLs, such as METTL3 and METTL14) catalyzing m6A methylation work in concert with the A-to-I editing enzymes, adenosine deaminase acting on RNA 1 (ADAR1) to drive malignant transformation of HSCs. By first exploring differentially expressed genes in lentiviral over-expressed ADAR1 hematopoietic cells and progenitor cells we observed downregulation in the m6A complex (i.e. METTL3, METTL14, and other METTLs), except METTL13. While METTL13 knockdown converged with the other m6A complex knockdown results in immune signaling and survival, METTL13 knockdown uniquely affected cancer related pathways compared to other METTLs. Using publicly available RNA sequencing data from TARGET, we determined that increased METTL13 expression, in both T cell ALL and B cell ALL correlated to poor patient prognosis. Additionally, functional studies for cell proliferation and survival, both in vitro and in vivo, demonstrated METTL13’s role in T-ALL when it is removed or lost. Overall these findings display the oncogenic role of METTL13 in T-ALL pathogenesis and pre-leukemic transformations, while revealing a continued research into this potential novel target for new therapies. Citation Format: Sabina Enlund, Chae-Eun Lim, Isabella Hoang, Sonali Joshi, Amanda Ramilo Amor, Cecilia Thomsson, Maria Rivera, Adena Pepich, Indranil Sinha, Shahrzad S. Fard, Anna Nilsson, Ola Hermanson, Qingfei Jiang, Frida Holm. Revealing the transformative role of METTL13 in human hematopoietic stem cells and progression of pediatric leukemia [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 1162.

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Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-1162
Primary Topic
RNA modifications and cancer
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article
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article

Abstract 1162: Revealing the transformative role of METTL13 in human hematopoietic stem cells and progression of pediatric leukemia

Sonali Joshi, Qingfei Jiang, Frida Holm, Shahrzad Shirazi Fard et al.
Cancer Research
RNA modifications and cancer
article

Abstract 1162: Revealing the transformative role of METTL13 in human hematopoietic stem cells and progression of pediatric leukemia

Sonali Joshi, Qingfei Jiang, Frida Holm, Shahrzad Shirazi Fard, Amanda Ramilo Amor, Indranil Sinha, M Gonzalez Rivera, Ola Hermanson, Sabina Enlund, Anna Nilsson, Adena Pepich, Chae-Eun Lim, Isabella Hoang, Cecilia Thomsson
article en

Abstract

Abstract Childhood leukemia’s five year survival rate has been improving over the last 40 years, but still only reaches 86.3% relative survival in the United States according to the Surveillance, Epidemiology, and End Results (SEER) program in 2025. Aberrant post-transcriptional RNA modifications, specifically N6-methyladenosine (m6A) methylation and adenosine to inosine (A-to-I) editing have previously been shown to push malignant transformations of hematopoietic stem cells (HSC). In order to unravel the mechanism behind these RNA modifiers and decipher whether methyltransferases (METTLs, such as METTL3 and METTL14) catalyzing m6A methylation work in concert with the A-to-I editing enzymes, adenosine deaminase acting on RNA 1 (ADAR1) to drive malignant transformation of HSCs. By first exploring differentially expressed genes in lentiviral over-expressed ADAR1 hematopoietic cells and progenitor cells we observed downregulation in the m6A complex (i.e. METTL3, METTL14, and other METTLs), except METTL13. While METTL13 knockdown converged with the other m6A complex knockdown results in immune signaling and survival, METTL13 knockdown uniquely affected cancer related pathways compared to other METTLs. Using publicly available RNA sequencing data from TARGET, we determined that increased METTL13 expression, in both T cell ALL and B cell ALL correlated to poor patient prognosis. Additionally, functional studies for cell proliferation and survival, both in vitro and in vivo, demonstrated METTL13’s role in T-ALL when it is removed or lost. Overall these findings display the oncogenic role of METTL13 in T-ALL pathogenesis and pre-leukemic transformations, while revealing a continued research into this potential novel target for new therapies. Citation Format: Sabina Enlund, Chae-Eun Lim, Isabella Hoang, Sonali Joshi, Amanda Ramilo Amor, Cecilia Thomsson, Maria Rivera, Adena Pepich, Indranil Sinha, Shahrzad S. Fard, Anna Nilsson, Ola Hermanson, Qingfei Jiang, Frida Holm. Revealing the transformative role of METTL13 in human hematopoietic stem cells and progression of pediatric leukemia [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 1162.

Cancer ResearchVol. 86(7_Supplement)
Karolinska Institutet (SE), University of California San Diego (US), Svenska Örtmedicinska Institute (SE)
Good health and well-being
Openalex Percentile: Top 8%
RNA modifications and cancer
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