Our previous studies revealed a decrease in lamin B1 expression28 and an increased expression of p1623 in deep infiltrative endometriosis lesions compared to that in the eutopic endometrium, which could potentially be implicated in the pro-senescence pattern of endometriosis lesions as both lamin b1 and p16 are biomarkers used to assess cellular senescence. Here, CDKN2A is linked to endometriosis.