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March 14, 2026APOPTOSIS7 citationsOpen Access

Looking at the fraction with Annexin V⁺ and propidium iodide⁺: insights into cell death types from preclinical studies in solid and haematological cancers

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SHSiti Nazihahasma HassanFAFaheem Ahmad

Key Points

  • To clarify the implications of double-positive cell populations identified through annexin V and propidium iodide in cancer research.
  • Collated findings from preclinical studies on solid and haematological cancers
  • Evaluated the use of annexin V and propidium iodide assays for understanding cell death types
  • Suggested the need for standardisation in interpreting annexin V⁺/PI⁺ populations
  • Identified various modalities of regulated cell death in the annexin V⁺/PI⁺ fraction
  • Emphasized the inadequacy of existing criteria for classifying late-stage cell death
  • Proposed the adoption of standardised interpretive criteria for better cross-study comparability

Abstract

Fluorescein isothiocyanate-conjugated Annexin V in combination with propidium iodide (PI) labelling is a widely used flow cytometric assay for quantifying apoptotic and necrotic cells in anticancer studies. However, increasing evidence suggests that double-positive cells, or the Annexin V⁺/PI⁺ fraction, may represent not only late apoptosis but also different modalities of regulated cell death, including necroptosis, pyroptosis, ferroptosis, and cuproptosis. By collating findings from preclinical studies across different cancer cells, this review highlights the need for consensus in interpreting Annexin V⁺/PI⁺ populations. In the absence of molecular and/or microscopy data, this fraction is more appropriately classified as undergoing 'late-stage cell death'. In short, establishing standardised interpretive criteria is crucial to enhance understanding, facilitate cross-study comparability, and improve the translational relevance of anticancer research.

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Cite This Study

Hassan et al. (2026) studied this question.

synapsesocial.com/papers/69b4ba3618185d8a39802f3ahttps://doi.org/10.1007/s10495-026-02261-x
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