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Blood biomarkers for inflammatory breast cancer (Level B2) — green pink and purple plastic bottles

Blood biomarkers for inflammatory breast cancerCEFR B2

22 May 2026

Level B2 – Upper-intermediate
5 min
269 words

Scientists have identified blood-based biomarkers that can reliably distinguish inflammatory breast cancer (IBC) from other breast cancer subtypes, a finding published in Science Advances. The study used Thermostable Group II Intron Reverse Transcriptase (TGIRT) sequencing, a method developed by Alan Lambowitz’s team at The University of Texas at Austin. TGIRT uses a more robust enzyme that tolerates extreme conditions and captures complex, fragmented RNAs that standard methods often miss.

Clinical samples and medical insights were provided by Savitri Krishnamurthy at The University of Texas MD Anderson Cancer Center and Naoto Ueno, then a professor at the Morgan Welch Inflammatory Breast Cancer Program and Clinic at UT MD Anderson and now director of the University of Hawai’i Cancer Center. The researchers also developed analytic methods to focus on protein-coding genes specific to IBC tumors.

Key findings include higher levels of noncoding RNAs and increased white blood cell counts in IBC patient blood compared with healthy or non-IBC patients. In plasma, IBC samples contained many intron RNA fragments, while healthy plasma mostly carried mRNA fragments. This pattern points to immune activation and imbalances in RNA splicing that reduce mRNA production. Overall, the team proposed several potential blood-based biomarkers that could improve diagnosis, monitoring and the development of new therapies. The work was funded by the National Institutes of Health, The Welch Foundation, the Breast Cancer Research Foundation, the UT MD Anderson Morgan Welch Inflammatory Breast Cancer Research Program and Clinic, and the State of Texas Rare and Aggressive Breast Cancer Research Program; a full list of authors and disclosures is available with the paper in Science Advances.

Difficult words

  • biomarkermolecule in blood used to detect disease
    biomarkers
  • reverse transcriptaseenzyme that makes DNA from RNA
  • thermostableable to work at high temperatures
  • noncoding RNARNA molecules that do not code proteins
    noncoding RNAs
  • intronsection of RNA removed during processing
  • splicingprocess that joins and removes RNA parts
  • immune activationstimulation of the body's immune response

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Discussion questions

  • How could blood-based biomarkers change diagnosis or monitoring for patients with inflammatory breast cancer?
  • What advantages might thermostable enzymes like TGIRT offer for sequencing in clinical tests?
  • What practical challenges could arise when turning these research findings into routine blood tests?

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