Correlation between senescence markers, such as IL-17A, p16Ink4a, lamin b1, IL-1α, and IL-2 and endometriosis have been observed.(25,27) Additionally, increased levels of IL-1β and IL-4 were detected in endometriotic lesions compared with that in the eutopic endometrium. Here, CDKN2A is linked to endometriosis.