2020
DOI: 10.1155/2020/6387545
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Suppression of KIF22 Inhibits Cell Proliferation and Xenograft Tumor Growth in Tongue Squamous Cell Carcinoma

Abstract: Background. Oral carcinoma is the sixth most common cancer and is a serious public health problem, and tongue squamous cell carcinoma (TSCC) is the most common type of oral carcinoma. Kinesin family member 22 (KIF22), also called as kinesin-like DNA binding protein (KID), is a microtubule-based motor protein and binds to both microtubules and chromosomes, transporting organelles, protein, and mRNA. This research aimed at investigating the prognostic significance of KIF22 in TSCC. Patients and Methods. This ret… Show more

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Cited by 6 publications
(8 citation statements)
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“…Several studies have identified KIF22 as an oncogene [ 17 , 20 23 ]. Here, we explored the function of KIF22 in glioma cells.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…Several studies have identified KIF22 as an oncogene [ 17 , 20 23 ]. Here, we explored the function of KIF22 in glioma cells.…”
Section: Resultsmentioning
confidence: 99%
“…In prostate cancer patients, high KIF22 expression is correlated with tumor development and poor prognosis [ 20 ]. Studies of KIF22 functions in breast cancer, gastric cancer, and tongue SCC have also been reported [ 21 23 ].…”
Section: Introductionmentioning
confidence: 99%
“…MAL PDT downregulated genes associated with proliferation, such as cyclins and the kinesin family member (KIF) proteins, and were similarly identified in our testing with a p < 0.05. KIF proteins are involved with microtubule organization during mitosis and have been previously found to be associated with cancer [28][29][30][31]. Knockdown of KIF22 inhibits tongue SCC proliferation and xenograft tumor growth [28].…”
Section: Discussionmentioning
confidence: 99%
“…KIF proteins are involved with microtubule organization during mitosis and have been previously found to be associated with cancer [28][29][30][31]. Knockdown of KIF22 inhibits tongue SCC proliferation and xenograft tumor growth [28]. In laboratory studies, PDT treatment protocols decreased cSSC tumor proliferation and increased apoptosis and autophagy via regulation of MAPK protein, particularly AKT [20][21][22].…”
Section: Discussionmentioning
confidence: 99%
“…HSPB7 promoter primers were detailed as follows: forward, -CATAGGCCAGTGATGAAGCC--GCTCTGCTGACCCTAACTCTT-Subcutaneous tumorigenesis experiment in nude mice . Referring to the previously reported methods [34,35], eighteen SPF-grade male BALB/c nude mice (5 weeks, 15~18 g) were randomly assigned into three groups: Control+sh-NC group, NaB+sh-NC group, and NaB+sh-HSPB7 group, with six mice in each group. SCC-15 cell suspension at a concentration of about 1 × 10 7 cells/ml was injected into the skin of the left axilla of nude mice with a 1 ml syringe to establish a nude mouse subcutaneous transplantation tumor model.…”
Section: Western Blot (Wb) Tissues or Cells Were Collected By Trypsin...mentioning
confidence: 99%