Evidence map›Paper›PMID 40017656›Full record

ArticlePeerJ2025

Alteration of primary cilia and intraflagellar transport 20 (IFT20) expression in oral squamous cell carcinoma (OSCC) cell lines.

Gulam Sakinah-Syed, Jia Shi Liew, Nazia Abdul Majid, Siti Amalina Inche Zainal Abidin

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Article in PeerJ, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Gulam Sakinah-SyedInstitute of Biological Sciences, Faculty of Science, Universiti Malaya, Kuala Lumpur, WP Kuala Lumpur, Malaysia.
Jia Shi LiewInstitute of Biological Sciences, Faculty of Science, Universiti Malaya, Kuala Lumpur, WP Kuala Lumpur, Malaysia.
Nazia Abdul MajidInstitute of Biological Sciences, Faculty of Science, Universiti Malaya, Kuala Lumpur, WP Kuala Lumpur, Malaysia.
Siti Amalina Inche Zainal AbidinDepartment of Oral & Craniofacial Sciences, Faculty of Dentistry, Universiti Malaya, Kuala Lumpur, WP Kuala Lumpur, Malaysia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Aberrations in primary cilia expression and intraflagellar transport (IFT) protein function have been implicated in tumourigenesis. This study explores the relationship between the alteration of primary cilia and tumourigenesis by investigating primary cilia expression and the role of IFT20 in regulating matrix metalloproteinase 9 (MMP-9) expression in oral squamous cell carcinoma (OSCC) cell lines. Methods: The frequency and length of primary cilia were determined in OKF6-TERT2 cells, HSC-2 cells, and HSC-3 cells using immunofluorescence. Additionally, primary cilia presence in non-proliferating OSCC cells was examined. OSCC cells were treated with either small interfering RNA (siRNA) negative control or siRNA targeting IFT20 for functional analysis. mRNA expression levels of IFT20 and MMP-9 were quantified using quantitative reverse transcription polymerase chain reaction (qRT-PCR). Results: Results showed that HSC-2 cells exhibit abundant primary cilia when cultured in low serum media (2% serum) for 48 h, followed by serum starvation for over 72 h. No significant changes in cilia expression were observed in HSC-3 cells compared to OKF6-TERT2 cells. Ciliated cells were found in non-proliferating HSC-2 and HSC-3 cells. OSCC cells showed longer cilia than OKF6-TERT2 cells, indicating ciliary abnormalities. Changes in ciliation and cilium length of OSCC cells were accompanied by increased expression of IFT20, an intraflagellar transport protein crucial for the primary cilia assembly. However, IFT20 knockdown did not affect MMP-9 at the mRNA level in these cells. Conclusions: This study reveals the differences in primary cilia expression among OSCC cells. Furthermore, the increased abundance and elongation of primary cilia in OSCC cells are accompanied by elevated expression of IFT20. Nonetheless, IFT20 did not affect MMP-9 mRNA expression in OSCC cells.

Indexed as

Carcinoma, Squamous CellCarrier ProteinsCiliaMouth NeoplasmsCell Line, TumorGene Expression Regulation, NeoplasticHumansMatrix Metalloproteinase 9RNA, MessengerRNA, Small InterferingCarrier ProteinsMatrix Metalloproteinase 9MMP9 protein, humanRNA, MessengerRNA, Small InterferingArl13bCilia lengthCilia occurrenceIFT20MMP-9Oral cancerPrimary cilia

Identifiers

PMID40017656
PMCPMC11867036

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.