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Abstract
CRISPR-Cas9-mediated deletion of the HERV-K102 envelope (K-Env) induces apoptosis and pyroptosis in acute myeloid leukemia cells.
- The deletion of K-Env activates the S100A9/NLRP3 inflammasome.
- Concerns exist regarding the evidence for distinguishing pyroptosis from secondary necrosis.
- A mechanistic rescue experiment is needed to confirm S100A9's role as a primary driver.
- The specificity of primers used at the mRNA level raises questions about the findings.
- The immunocompromised xenograft model may not accurately represent immune evasion associated with K-Env.
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