CKIP-1 silencing suppresses OSCC via mitochondrial homeostasis-associated TFAM/cGAS-STING signalling axis

J Cell Mol Med. 2024 Aug;28(16):e70006. doi: 10.1111/jcmm.70006.

Abstract

Limited effective targets have challenged the treatment of oral squamous cell carcinoma (OSCC). Casein kinase 2 interacting protein 1 (CKIP-1) is a scaffold protein involved in various diseases. However, the role of CKIP-1 in OSCC remains unclear. The aim of this study was to explore the regulatory role of CKIP-1 in OSCC, as well as the involved mechanism. First, higher expression of CKIP-1 in OSCC tissues and cell lines were found. Series of gain- and loss-of-function experiments demonstrated suppressed malignant behaviours and enhanced apoptosis of OSCC cells when CKIP-1 was silenced. Also, inhibited tumour growth in CKIP-1-silenced group were proved. Further, mitochondrial transcription factor A (TFAM) downregulation, increased ROS production, decreased mitochondrial membrane potential and cGAS-STING activation in CKIP-1-silenced group were observed. The involvement of mitochondrial homeostasis-related TFAM/cGAS-STING axis in CKIP-1-silenced OSCC cells was finally demonstrated by tetramethylpyrazine (TMP) that inhibits TFAM degradation. Taken together, our study demonstrated that CKIP-1 silencing could significantly antagonize OSCC via TFAM/cGAS-STING axis, which may provide a candidate target for OSCC treatment.

Keywords: gene therapy; mitochondria; oral squamous cell carcinoma; signal transduction.

MeSH terms

  • Animals
  • Apoptosis*
  • Carcinoma, Squamous Cell* / genetics
  • Carcinoma, Squamous Cell* / metabolism
  • Carcinoma, Squamous Cell* / pathology
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism
  • Cell Line, Tumor
  • Cell Proliferation
  • DNA-Binding Proteins* / genetics
  • DNA-Binding Proteins* / metabolism
  • Gene Expression Regulation, Neoplastic
  • Gene Silencing
  • Homeostasis
  • Humans
  • Intracellular Signaling Peptides and Proteins
  • Male
  • Membrane Potential, Mitochondrial / drug effects
  • Membrane Proteins* / genetics
  • Membrane Proteins* / metabolism
  • Mice
  • Mitochondria* / drug effects
  • Mitochondria* / metabolism
  • Mitochondrial Proteins / genetics
  • Mitochondrial Proteins / metabolism
  • Mouth Neoplasms* / genetics
  • Mouth Neoplasms* / metabolism
  • Mouth Neoplasms* / pathology
  • Reactive Oxygen Species / metabolism
  • Signal Transduction*
  • Transcription Factors* / genetics
  • Transcription Factors* / metabolism

Substances

  • Membrane Proteins
  • Transcription Factors
  • DNA-Binding Proteins
  • TFAM protein, human
  • STING1 protein, human
  • PLEKHO1 protein, human
  • Mitochondrial Proteins
  • Carrier Proteins
  • Reactive Oxygen Species
  • Intracellular Signaling Peptides and Proteins