The functionality of STING protein is regulated by a variety of post‐translational modifications, which are critical for its stability, activity and immune response modulation.[29] To explore the mechanisms underlying the post‐translational modification regulation of STING proteins in cervical cancer, immunoprecipitation‐mass spectrometry (IP‐MS) was employed to explore the crucial binding partners of STING proteins. The gene discussed is STING1; the disease is cervical cancer.