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Previous studies have suggested that cancer stem cells (CSCs) resisted radiotherapy and chemotherapy. P16 INK4A is a biomarker for cervical carcinogenesis and reduces proliferation of stem cells. We aimed to investigate the expression and clinical significance of cyclin-dependent kinase inhibitor 2A (P16 INK4A ), sex determining region Y-box 2 (SOX2), and Aldehyde dehydrogenase 1 family, member A1 (ALDH1A1) in cervical cancer treated with radiotherapy and cervical cell line models. The expressions of P16 INK4A , SOX2, and ALDH1A1 were performed by immunohistochemical staining of tumor samples from 139 cervical cancer patients with International Federation of Gynecology and Obstetrics stages Ib to IV. The staining showed high expression in 100, 107, and 13 patients with P16 INK4A (&gt;80%), SOX2 (≥10%), and ALDH1A1 (50%), respectively. The high-P16 INK4A group had a higher five-year overall survival (OS) rate and disease-free survival (DFS) than the low-P16 INK4A group (OS: 62.0% and 35.2%, p = 0.016; DFS: 60.0% and 31.2%, p = 0.002). The low-P16 INK4A /high-SOX2 and low-P16 INK4A /high-ALDH1A1 groups had a worse five-year OS and DFS rate than the high-P16 INK4A /low-SOX2 and high-P16 INK4A /low-ALDH1A1 groups, respectively. Depletion of P16 INK4A promoted chemoresistance and radioresistance of cervical cancer cells increased the expression of SOX2 and ALDH1A1 and exhibited higher self-renewal ability. These results suggest that lower P16 INK4A expression associated with higher CSC markers predicts poor prognostic outcomes and is a promising target in patients with cervical cancer.

Low P16INK4A Expression Associated with High Expression of Cancer Stem Cell Markers Predicts Poor Prognosis in Cervical Cancer after Radiotherapy