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High-throughput assay confirmation of a T-cell receptor pre-mRNA fragment as a blood-based inflammatory breast cancer biomarker

Ferrick-Kiddie, E. A.; Dommaraju, S.; Yao, J.; Smith, C. W.; Wang, X.; Woodward, W. A.; The MDACC Inflammatory Breast Cancer Team, ; Ueno, N. T.; Krishnamurthy, S.; Lambowitz, A. M.

2025-08-21 oncology
10.1101/2025.08.19.25333925 medRxiv
Show abstract

Previous TGIRT-seq analysis of RNAs in Inflammatory Breast Cancer (IBC) patient tumors, peripheral blood mononuclear cells (PBMCs) and plasma identified a short T-cell receptor mRNA fragment (TRBJ1-6) as a potential IBC biomarker that was detected in plasma samples from IBC patients but not patients with non-inflammatory breast cancer or healthy donors. Here, we traced the origin of this TRBJ1-6 RNA fragment to IBC patient PBMCs and used a high-throughput RT-PCR/Cas12a assay with larger numbers of samples to confirm its prevalence in IBC patient PBMCs. Detection of this RNA was enhanced by T4 polynucleotide kinase treatment, indicating the presence of a 2,3-cyclic phosphate. Analysis of previous TGIRT-seq datasets revealed gene expression differences in IBC patient PBMCs that could contribute to TRBJ1-6 RNA prevalence in IBC patient PBMCs and plasma. Our results support the identification of the TRBJ1-6 RNA fragment as a novel, readily detectable blood-based RNA biomarker derived from IBC-patient immune cells, addressing a major unmet need for diagnosing IBC. TeaserA novel type of blood-based biomarker for diagnosis of Inflammatory Breast Cancer

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