Phosphorylation of histone H2AX as a marker of dsDNA breaks induced from cell internalization of Dato-DΧd. A, TROP2-negative cell line END(K)34 does not show statistically significant difference in p-H2AX MFI when treated with 5 μg/mL Dato-DΧd vs. when treated with 5 μg/mL control ADC (P > 0.05). B and C, Increase in p-H2AX MFI is statistically significant when high (3+) TROP2-expressing cell lines END(K)254 and END(K)265 are treated with 5 μg/mL Dato-DΧd vs. 5 μg/mL control ADC (P = 0.0156 and P = 0.0427; *, P
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Niccolò G. Santin
Namrata Sethi
Stefania Bellone
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Santin et al. (Thu,) studied this question.
www.synapsesocial.com/papers/68d44b3031b076d99fa5492b — DOI: https://doi.org/10.1158/2767-9764.30102515