Introduction
Oral squamous cell carcinoma (OSCC) is a disease with increasing incidence worldwide that leads to deformity and death [
1]. Recently, the incidence and mortality rates of OSCC are increasing worldwide, and this increase in mortality rate is associated with regional and distant metastasis, which leads to a worse prognosis [
2]. Despite improvements in OSCC diagnosis and treatment, almost half of patients with OSCC die within five years of diagnosis [
3]. Improving our understanding of the complex process of OSCC could provide additional opportunities to improve treatment and patient prognosis.
Fascin actin-bundling protein 1 (FSCN1) belongs to the fascin family of proteins that bind to actin [
4]. FSCN1 serves as an important regulator in cell migration and cell-to-cell interactions [
5,
6]. Overexpression of FSCN1, which promotes cell migration, has been reported to be associated with cancer metastasis in many studies [
7]. For example, in ovarian cancer, FSCN1 promotes epithelial-mesenchymal transition (EMT) by interacting with and increasing the expression levels of snail1 [
8]. In hepatocellular carcinoma, FSCN1 is overexpressed, and by promoting EMT, FSCN1 increases the chemoresistance capacity of hepatocellular carcinoma [
9].
In OSCC, FSCN1 is identified as an oncogene involved in the tumorigenesis process. Amplification and mRNA upregulation of FSCN1 was found in OSCC [
10]. In addition, FSCN1 expression levels were related to the prognosis of patients with OSCC, and patients with high FSCN1 expression had poorer outcomes than patients with low FSCN1 expression [
11]. There are, however, no reports on the functions and potential mechanisms of FSCN1 in OSCC tumorigenesis.
In this study, we aimed to examine the expression patterns of FSCN1 in OSCC cell lines and tissues as well as its biological functions in processes including proliferation, invasion, and glycolysis. Moreover, we investigated the underlying mechanisms by which FSCN1 functions in the OSCC tumorigenesis process, which should shed some light on the potential of FSCN1 as a diagnostic biomarker and therapeutic target molecule for OSCC.
Materials and methods
Cell culture
Human normal oral keratinocytes (HNOK) and human OSCC cell lines (SCC9, SCC15, SCC25, HN4, HSC3, HSC6 and CAL27) were purchased from ATCC (USA) and maintained at 37 °C and 5% CO2. Cells were grown in DMEM (HyClone) supplemented with 10% FBS (Gibco). Mycoplasma infection and cell line authenticity were verified by DNA fingerprinting before use.
Tissue specimens
Forty paired OSCC tissue specimens (Tumor) and neighboring noncancerous tissue specimens (Normal) were obtained during surgery at Sun Yat-sen University Cancer Center. Fresh tissues were stored in TRIzol (Invitrogen, USA) immediately after being cut and were used for subsequent qRT‒PCR assays. In accordance with its ethical approval, this study was conducted at Sun Yat-sen University Cancer Center and was carried out in accordance with the Declaration of Helsinki. Written informed consent was provided by all patients.
qRT‒PCR
Total OSCC cell and tissue RNA was obtained by TRIzol (Invitrogen). With the SYBR Premix Ex Taq kit (Takara, China), mRNA expression was detected on an Applied Biosystems 7500 Fast Real-Time PCR System. The following primers were synthesized by Life Technologies: FSCN1 forward, 5’-CCAGGGTATGGACCTGTCTG-3’, reverse, 5’-GTGTGGGTACGGAAGGCAC-3’; GAPDH forward, 5’-ACAACTTTGGTATCGTGGAAGG-3’, reverse, 5’-GCCATCACGCCACAGTTTC-3’. The relative gene expression levels were calculated with the 2−ΔΔCT formula with GAPDH as the internal reference.
Cell transfection
Briefly, si-FSCN1#1 (5’-GCGCCUACAACAUCAAAGA-3’), si-FSCN1#2 (5’-GCCCAUGAUAGUAGCUUCA-3’), si-FSCN1#3 (5’-GCAGCCUGAAGAAGAAGCA-3’) or the appropriate control si-NC (GeneCopoeia, USA) was transiently transfected into the SCC15 and HSC3 cell lines (Lipofectamine 3000, Invitrogen). The cells were collected and subjected to further experiments 48 h later.
ShRNA construction and lentiviral infection
GeneCopoeia synthesized FSCN1 shRNAs, and the Lenti-PacTM HIV Expression Packaging Kit (GeneCopoeia) was used to generate lentiviruses expressing sh-FSCN1. SCC15 and HSC3 cell lines were infected with lentiviruses using Lipo3000. SCC15-sh-FSCN1 and HSC3-sh-FSCN1 cells were selected with puromycin (2 µg/mL) and subjected to further experiments.
CCK-8 assay
SCC15-sh-FSCN1 cells, HSC3-sh-FSCN1 cells and control cells were seeded in 96-well plates (3000 cells/well). Forty-eight hours later, 10 µl CCK-8 solution (Dojindo, Japan) was added. Finally, the absorbance at 450 nm was detected 2 h later using a microplate reader.
SCC15-sh-FSCN1 cells, HSC3-sh-FSCN1 cells and control cells were seeded in six-well plates (1000 cells/well). Fourteen days later, methanol was used to fix the colonies for 30 min, and crystal violet (0.1%) was used to stain them for 30 min. The number of colonies was counted and averaged in three independent experiments.
Transwell assay
SCC15-sh-FSCN1 cells, HSC3-sh-FSCN1 cells and control cells were resuspended in serum-free medium and seeded into 24-well transwell chambers (1 × 104 cells/well) precoated with Matrigel (BD Bioscience, USA) for the invasion assay. A 20% FBS solution was added to the lower chamber, while medium without FBS was added to the upper chamber. After 24 h of incubation, the invaded cells were fixed with cold methanol, and crystal violet (0.1%) was used to stain the invaded cells for 20 min. The number of invaded cells was quantified in five randomly selected fields under a light microscope.
Glucose consumption was detected by the Glucose Test Kit (Biovision, USA). SCC15-sh-FSCN1 cells, HSC3-sh-FSCN1 cells and control cells were seeded (1 × 10
6 cells/well each), and glucose concentration reduction was detected with cell culture medium. Similarly, lactate production was investigated with the Lactate Assay Kit (Biovision). The ATP/ADP ratio was detected by the ApoSENSOR ADP/ATP Ratio Assay Kit (Biovision) [
12].
Western blotting
Total OSCC cell proteins were extracted with PMSF and RIPA lysis buffer (Sigma, USA), and the protein concentration was determined with a Pierce BCA protein assay kit. Proteins were subjected to 12% SDS‒PAGE and transferred onto a PVDF membrane. The membrane was blocked with 5% skim milk powder for 2 h at room temperature. Then, primary antibodies against the following proteins were added for incubation overnight at 4 °C: FSCN1 (1:1000, #ab126772, Abcam, USA), IRF4 (1:500, #sc-6059, Santa Cruz Biotechnology, USA), AKT (1:500, #9272, CST, USA), p-AKT (1:500, #9271, CST), E-cadherin (1:1000, #3195, CST), Vimentin (1:1000, #5741, CST) and GAPDH (1:1000, #AF7021, Affinity, USA). Next, the membrane was incubated with HRP-linked secondary antibody (1:3000, #7074S, CST) for 2 h at room temperature. The final step in the process was to visualize and quantify the target proteins (ECL New England Biolabs, USA), and relative grayscale quantification was conducted with ImageJ software. The blots were cut prior to hybridization with antibodies. The original western blotting images are provided in the Supplementary Data.
Statistical analysis
All experiments were repeated at least three times. Analyses were conducted using GraphPad Prism 9.0 software. For paired continuous variables in homologous pairing design, we conduct a normality test on the difference of paired variables using the Shapiro-Wilk test. T tests and one-way variance analyses were employed. All data are presented as the mean ± standard deviation. Statistics are considered significant when P ≤ 0.05.
Discussion
OSCC is indeed the most common cancer in the oral cavity worldwide, and it has a poor prognosis and a high mortality rate [
17]. Even with recent advances in treatments, such as targeted drugs and immunotherapy, the long-term prognosis is poor. Due to the limited treatment options for late-stage OSCC, the survival outcome is poor due to cancer metastasis, recurrence and drug resistance [
18]. Hence, we need more comprehensive investigations of the mechanism of OSCC tumorigenesis to explore effective treatments to improve the outcome of OSCC.
FSCN1 is upregulated in multiple cancers and is related to cancer metastasis and a poor prognosis [
19‐
22]. In OSCC, FSCN1 is also upregulated and associated with advanced clinical stage [
23,
24]. So far, there have been only a few studies that involve the role of FSCN1 in OSCC. FSCN1 has been reported to regulate migration [
25] and cell–cell contact [
26] to promote OSCC progression. However, the exact mechanisms of FSCN1 deregulation and functions in OSCC are still under investigation. Further experimental verification is needed. Here, we investigated FSCN1 expression patterns in OSCC cells as well as tissues and found that OSCC cells expressed high levels of FSCN1 (Fig.
1). Subsequent functional experiments revealed that FSCN1 inhibition suppressed OSCC cell proliferation and invasion (Fig.
2).
Emerging studies have demonstrated that the molecular pathogenesis of OSCC is complex, involving dysregulated metabolites [
27], which is one of the hallmarks of cancer [
28]. The Warburg effect is observed in OSCC due to the requirement of a robust glucose supply to fuel cancer growth and proliferation [
29,
30]. Hypoxia-related glucose metabolism, also known as glycolysis, is correlated with OSCC carcinogenesis. Inhibition of glycolysis might therefore serve as a potential adjuvant strategy in OSCC [
31].
FSCN1 has been reported to increase cell glycolysis to promote tumor growth and metastasis through the YAP1-PFKFB3 axis in lung cancer [
32]. However, the functions of FSCN1 in the OSCC glycolysis process have not yet been reported. Here, we showed that FSCN1 inhibition suppressed OSCC glycolysis by decreasing glucose consumption levels, lactate production levels and the ATP/ADP ratio (Fig.
3). All the above results illustrate that FSCN1 plays an essential role in the OSCC glycolysis process.
Next, we further investigated the mechanism involving FSCN1 in OSCC progression. Through bioinformatics analysis, we found that FSCN1 could interact with IRF4, which is involved in the oncogenesis of multiple cancers. For instance, IRF4 upregulation was correlated with survival outcomes in head and neck squamous carcinoma [
33]. In cholangiocarcinoma, IRF4 promotes cancer proliferation as well as metastasis by regulating PI3K/AKT signaling [
34]. However, no research has focused on the relationship between FSCN1 and IRF4 in OSCC thus far. Here, we revealed that FSCN1 silencing markedly decreased the IRF4 expression level in OSCC cells (Fig.
4).
In esophageal squamous cell carcinoma, FSCN1 was reported to promote tumor progression by the AKT/GSK3β signaling pathway [
35]. Moreover, in lung adenocarcinoma, FSCN1 promotes tumor development through PI3K/AKT signaling [
36]. Notably, in OSCC, PGK1 promotes cell glycolysis and EMT by activating AKT signaling [
37]. B7-H3 promotes OSCC progression and the glycolytic metabolic program via PI3K/Akt/mTOR signaling [
38]. However, the relationship between FSCN1 and AKT in OSCC has not yet been reported. In this study, we showed that FSCN1 knockdown decreased phosphorylated AKT levels, showing that FSCN1 may contribute to OSCC progression partly through an AKT-dependent pathway (Fig.
4).
In summary, our study revealed the important role that FSCN1 plays in OSCC. FSCN1 is overexpressed and acts as a promoter of OSCC proliferation, invasion, and glycolysis partially via IRF4-Akt signaling activation. Hence, it is possible that FSCN1 could be used as a treatment target as well as a biomarker for OSCC. Further research is needed to validate and optimize these findings for the future development of an FSCN1-targeted strategy for OSCC.
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