Increased expression levels of transforming growth factor-β1 (TGF-β1) are associated with metastasis in papillary thyroid carcinoma (PTC), although the mechanisms involved remain unknown. The present study aimed to investigate these mechanisms. The results demonstrated that the expression levels of TGF-β1 mRNA were higher and those of lncRNA-NEF were lower in tumor tissues compared with in healthy tissues. High levels of TGF-β1 mRNA and low levels of lncRNA-NEF were also detected in the serum of patients with PTC compared with in healthy controls. Serum levels of TGF-β1 and lncRNA-NEF were significantly associated with lymph node metastasis. Furthermore, TGF-β1 promoted cell migration and invasion of PTC cell lines, but not the normal cell line, whereas lncRNA-NEF overexpression inhibited these phenomena. TGF-β1 also inhibited lncRNA-NEF expression in PTC cell lines, but not in the normal cell line. Conversely, lncRNA-NEF overexpression exhibited no effects on TGF-β1. In conclusion, the present study suggested that TGF-β1 may promote the invasion and migration of PTC cells by inhibiting the expression of lncRNA-NEF.
Papillary thyroid carcinoma (PTC) is the most common type of thyroid cancer. It originates from follicular cells in the simple unicellular epithelium of the thyroid (
The expression levels of transforming growth factor-β1 (TGF-β1) are altered in patients with PTC and lymph node metastasis (
A total of 62 patients with PTC who were initially diagnosed and treated at the Affiliated Xinhua Hospital of Dalian University (Dalian, China) between January 2015 and January 2018 were included in this study. Patients with other types of malignancies, severe diseases and thyroid diseases, and patients who had received treatment prior to admission were excluded. The patients comprised 35 men and 27 women, aged between 22 and 72 years old, with a mean age of 45±9.8 years. Lymph node metastasis was found in 27 patients. In addition, 42 healthy volunteers were enrolled in this study, which represented the control group. The control group comprised 20 men and 22 women, aged between 24 and 69 years old, with a mean age of 44±10.2 years. No differences in age and sex were detected between the two groups. The study was approved by the Ethics Committee of the Affiliated Xinhua Hospital of Dalian University, and all patients provided written informed consent.
The present study included 62 patients with PTC, of which 40 received surgical tumor resection. During tumor resection, tumor tissues and adjacent healthy tissues were collected. All patients exhibited normal thyroid function prior to surgery, and none of them received radiotherapy or chemotherapy prior to admission to hospital. Blood (15 ml) was extracted from the elbow vein of all 62 patients with PTC and 42 healthy controls. Blood was maintained at room temperature for 2 h, followed by centrifugation at 1,087 × g for 20 min to collect serum. All tissues and serum were stored in liquid nitrogen for long-term use.
The present study used two human PTC cell lines, IHH-4 and HTH83, and the normal thyroid follicular epithelial cell line Nthy-ori 3-1 (all from American Type Culture Collection, Manassas, VA, USA). All cells were cultured in Dulbecco's modified Eagle's medium (Gibco; Thermo Fisher Scientific, Inc., Waltham, MA, USA) supplemented with 10% fetal bovine serum (Gibco; Thermo Fisher Scientific, Inc.), 100 U/ml streptomycin and 100 mg/ml penicillin G (Gibco; Thermo Fisher Scientific, Inc., Waltham, MA, USA) at 37°C in a humidified incubator containing 5% CO2. Cells treated with TGF-β1 (cat. no. T7039-2UG; Sigma-Aldrich; Merck KGaA, Darmstadt, Germany) were cultured in serum-free medium for 12 h. Cell treatment with TGF-β1 was performed at 10 ng/ml, for 24 h at 37°C as recommended by the supplier.
TRIzol® reagent (Invitrogen; Thermo Fisher Scientific, Inc.) was used to extract RNA from tissues and cells. Tumor tissues and adjacent healthy tissues were ground in liquid nitrogen prior to the addition of TRIzol® reagent. RNA samples were tested by NanoDrop™ 2000 Spectrophotometer (NanoDrop; Thermo Fisher Scientific, Inc., Wilmington, DE, USA), and RNA samples with an A260/A280 ratio between 1.8 and 2.0 underwent RT to synthesize cDNA using AMV reverse transcriptase (Gibco; Thermo Fisher Scientific, Inc.) according to the manufacturer's protocol. TaqMan PCR kit (Thermo Fisher Scientific, Inc.) was used to prepare PCR, and PCR reactions were carried out on a Bio-Rad iCycler (Bio-Rad Laboratories, Inc., Hercules, CA, USA). The primer sequences used for RT-qPCR were as follow: TGF-β1, forward 5′-GGCCTTTCCTGCTTCTCATGG-3′, reverse 5′-CCTTGCTGTACTGCGTGTCC-3′; lncRNA-NEF, forward 5′-CTGCCGTCTTAAACCAACCC-3′, reverse 5′-GCCCAAACAGCTCCTCAATT-3′; and GAPDH, forward 5′-CAGGAGGCATTGCTGATGAT-3′, reverse 5′-GAAGGCTGGGGCTCATTT-3′. PCR reaction conditions were as follow: 95°C for 50 sec, followed by 40 cycles at 95°C for 12 sec and 56°C for 35 sec. Relative expression levels of TGF-β1 and lncRNA-NEF were normalized to the endogenous control GAPDH using the 2−ΔΔCq method (
Full-length lncRNA-NEF cDNA (Sangon Biotech, Co., Ltd., Shanghai, China) with U6 promoter was inserted into a pcDNA3.1 vector (Sangon Biotech, Co., Ltd.) to establish a lncRNA-NEF expression vector. Lipofectamine® 2000 transfection reagent (cat no. 11668-019, Invitrogen; Thermo Fisher Scientific, Inc.) was used to transfect 5×105 cells with 10 nM vector. Transfection with an empty vector was used as a negative control. After 48 h, cells were collected for subsequent experiments. In cases of TGF-β1 treatment, TGF-β1 (10 ng/ml) was added at 24 h following transfection.
Cells collected during the logarithmic growth phase were used to prepare single cell suspensions at a final density of 5×104 cells/ml. In cases of TGF-β1 treatment, TGF-β1 (10 ng/ml) was added at 24 h after transfection, followed by migration and invasion assay. For the Transwell migration assay, 0.1 ml volume of the 5×104 cells/ml suspension was transferred to the upper chamber, and RPMI-1640 medium (Gibco; Thermo Fisher Scientific, Inc.) supplemented with 20% fetal calf serum (Sigma-Aldrich; Merck KGaA) was used to fill the lower chamber. After 24 h, membranes were collected and stained with 0.5% crystal violet (Sigma-Aldrich; Merck KGaA) at room temperature for 20 min. Prior to the invasion assay, the upper chamber was pre-coated with Matrigel (cat no. 356234; EMD Millipore, Billerica, MA, USA); all other steps were the same as for the migration assay. Cells were observed and counted under Olympus BH2 microscope (Tokyo, Japan).
Cell lysis buffer (cat no. P0013K; Beyotime Institute of Biotechnology, Haimen, China) was used to extract total protein from cells, and protein concentration was determined using the bicinchoninic acid assay. Proteins were separated by 10% SDS-PAGE with 30 µg per well and were transferred onto polyvinylidene difluoride membranes. Membranes were then blocked with 5% skimmed milk at room temperature for 1 h, prior to incubation with the following primary antibodies: Rabbit anti-TGF-β1 (1:2,000, cat no. ab9758; Abcam, Cambridge, UK) and rabbit anti-GAPDH (1:2,000, cat no. ab37168; Abcam) overnight at 4°C. After washing with Tris-buffered saline-0.3% Tween (TBST), membranes were incubated with anti-rabbit immunoglobulin G-horseradish peroxidase secondary antibody (1:1,000, cat no. MBS435036; MyBioSource, Inc., San Diego, CA, USA) at room temperature for 2 h. After washing with TBST, bands were detected using enhanced chemiluminescence substrate (Sigma-Aldrich; Merck KGaA). Relative expression levels of TGF-β1 were normalized to the endogenous control GAPDH using ImageJ V1.6 (National Institutes of Health, Bethesda, MD, USA).
Statistical analyses were performed using SPSS 19.0 (IBM Corp., Armonk, NY, USA). Experiments were performed in triplicate manner and data are presented as the means ± standard deviation. Comparisons between two groups were performed by un-paired t test, and comparisons among multiple groups were performed by one-way analysis of variance followed by Tukey's post-hoc test. Comparisons between tumor and adjacent healthy tissues were performed by a paired t-test. Pearson correlation coefficient analysis was performed to analyze the correlation between TGF-β1 mRNA and lncRNA-NEF expression. Associations of serum levels of TGF-β1 mRNA and lncRNA-NEF with clinicopathological data of patients were analyzed by χ2 test. Receiver operating characteristic (ROC) curve analysis was performed to evaluate the diagnostic values of serum TGF-β1 mRNA and lncRNA-NEF for patients with PTC and healthy controls. P<0.05 was considered to indicate a statistically significant difference.
The expression levels of TGF-β1 and lncRNA-NEF were detected in the tumor tissues and adjacent healthy tissues of 40 patients with PTC using RT-qPCR. As shown in
As shown in
ROC curve analysis was performed to evaluate the diagnostic values of serum TGF-β1 mRNA and lncRNA-NEF for PTC. The area under the curve (AUC) of serum TGF-β1 in the diagnosis of PTC was 0.9153 with a 95% confidence interval (CI) of 0.8644–0.9661 (P<0.0001;
According to the median serum levels of TGF-β1 mRNA and lncRNA-NEF, patients were divided into the high-expression and low-expression groups (n=31). The associations of serum levels of TGF-β1 mRNA and lncRNA-NEF with clinicopathological data of patients with PTC was analyzed by χ2 test. As shown in
In the present study, lncRNA-NEF overexpression reduced the enhancing effects of TGF-β1 on cell migration and invasion. To further investigate the interactions between TGF-β1 and lncRNA-NEF, IHH-4, HTH83 and Nthy-ori 3-1 cells were treated with TGF-β1 (10 ng/ml) and underwent lncRNA-NEF expression vector transfection. The expression levels of TGF-β1 (25 kD active homodimer) and lncRNA-NEF were then detected. As shown in
As determined in the present study, TGF-β1 and lncRNA-NEF were associated with tumor metastasis. In the present study, two human PTC cell lines, IHH-4 and HTH83, and the Nthy-ori 3-1 normal thyroid follicular epithelial cell line, were treated with TGF-β1 (10 ng/ml) and underwent lncRNA-NEF expression vector transfection. Cell migration and invasion were then detected by Transwell migration and invasion assays. As presented in
Since its pathogenesis is unclear, PTC is associated with a high rate of recurrence following treatment; therefore, research regarding the molecular pathogenesis and mechanisms underlying PTC is important (
Blood markers have been widely used in the early diagnosis of cancer (
The present study also revealed that the serum levels of TGF-β1 mRNA and lncRNA-NEF were closely associated with lymph node metastasis, but not tumor size, indicating their involvement in tumor metastasis. Transwell assays demonstrated that TGF-β1 promoted cell migration and invasion of IHH-4 and HTH83 cell lines, but not the Nthy-ori 3-1 cell line, whereas lncRNA-NEF overexpression had the opposite effects. These results suggested that TGF-β1 and lncRNA-NEF may be potential targets for the treatment of PTC. It is well known that the TGF-β pathway interacts with lncRNAs to achieve its biological functions (
In conclusion, in this study, TGF-β1 was upregulated, whereas lncRNA-NEF was downregulated in PTC. In addition, it was suggested that TGF-β1 and lncRNA-NEF may be considered potential reliable diagnostic markers for PTC. Furthermore, TGF-β1 promoted and lncRNA-NEF overexpression inhibited cell migration and invasion of PTC cell lines, but not the normal cell line. TGF-β1 also inhibited the expression levels of lncRNA-NEF in PTC cell lines but not in the normal cell line; however, lncRNA-NEF overexpression had no effect on TGF-β1 expression. These results suggested that TGF-β1 may promote the invasion and migration of PTC cells by inhibiting the expression of lncRNA-NEF.
Not applicable.
No funding was received.
The datasets used and/or analyzed during the present study are available from the corresponding author on reasonable request.
YW designed the experiments. JX performed all experiments. YL and XD analyzed data. And YW wrote the manuscript. All authors read and approved the final manuscript.
The study was approved by the Ethics Committee of the Affiliated Xinhua Hospital of Dalian University, and all patients provided written informed consent.
Patient signed informed consent for publication.
The authors declare that they have no competing interests.
Expression of TGF-β1 mRNA and lncRNA-NEF in PTC tissues and adjacent healthy tissues of patients with PTC. (A) Expression of TGF-β1 mRNA in tumor tissues and healthy tissues of patients with PTC. (B) Expression of lncRNA-NEF in tumor tissues and healthy tissues of patients with PTC. (C) TGF-β1 mRNA and lncRNA-NEF were negatively correlated in tumor tissues. (D) TGF-β1 mRNA and lncRNA-NEF were not significantly correlated in healthy tissues. *P<0.05 compared with adjacent healthy tissues. lncRNA-NEF, long non-coding RNA-neighboring enhancer of forkhead box A2; PTC, papillary thyroid carcinoma; TGF-β1, transforming growth factor-β1.
Expression of TGF-β1 mRNA and lncRNA-NEF in the serum samples of healthy controls and patients with PTC. (A) Expression of TGF-β1 in the serum of healthy controls and patients with PTC. (B) Expression of lncRNA-NEF in the serum of healthy controls and patients with PTC. (C) Serum TGF-β1 mRNA and lncRNA-NEF were negatively correlated in patients with PTC. (D) Serum TGF-β1 mRNA and lncRNA-NEF were not significantly correlated in healthy controls. *P<0.05. lncRNA-NEF, long non-coding RNA-neighboring enhancer of forkhead box A2; PTC, papillary thyroid carcinoma; TGF-β1, transforming growth factor-β1.
Diagnostic values of serum TGF-β1 mRNA and lncRNA-NEF for PTC. (A) ROC curve analysis of serum TGF-β1 in the diagnosis of PTC. (B) ROC curve analysis of serum lncRNA-NEF in the diagnosis of PTC. lncRNA-NEF, long non-coding RNA-neighboring enhancer of forkhead box A2; PTC, papillary thyroid carcinoma; ROC, receiver operating characteristic; TGF-β1, transforming growth factor-β1.
Possible interactions between TGF-β1 and lncRNA-NEF. (A) Effects of TGF-β1 treatment on lncRNA-NEF expression. (B) Effects of lncRNA-NEF overexpression on lncRNA-NEF and TGF-β1 (active form) expression. *P<0.05. C, control; lncRNA-NEF, long non-coding RNA-neighboring enhancer of forkhead box A2; NC, negative control; PTC, papillary thyroid carcinoma; TGF-β1, transforming growth factor-β1.
Effects of TGF-β1 treatment and lncRNA-NEF overexpression on cell migration and invasion. Migration and invasion of the two human PTC cell lines (A) IHH-4 and (B) HTH83, and (C) Nthy-ori 3-1normal thyroid follicular epithelial cells. *P<0.05. C, control; lncRNA-NEF, long non-coding RNA-neighboring enhancer of forkhead box A2; NC, negative control; PTC, papillary thyroid carcinoma; TGF-β1, transforming growth factor-β1 (×50 magnification).
Association between serum levels of TGF-β1 mRNA and clinicopathological data of patients.
Variable | Nο. | High-expression | Low-expression | χ2 | P-value |
---|---|---|---|---|---|
Sex | 0.59 | 0.44 | |||
Male | 35 | 16 | 19 | ||
Female | 27 | 15 | 12 | ||
Age (years) | 1.04 | 0.31 | |||
≥45 | 28 | 12 | 16 | ||
<45 | 34 | 19 | 15 | ||
Primary tumor diameter (cm) | 2.39 | 0.30 | |||
>4 | 26 | 16 | 10 | ||
2–4 | 17 | 7 | 10 | ||
<2 | 19 | 8 | 11 | ||
Lymph node metastasis | 7.94 | 0.010 | |||
Yes | 27 | 19 | 8 | ||
No | 35 | 12 | 23 | ||
Smoking | 0.58 | 0.45 | |||
Yes | 31 | 17 | 14 | ||
No | 31 | 14 | 17 | ||
Drinking | 0.27 | 0.6 | |||
Yes | 38 | 20 | 18 | ||
No | 24 | 11 | 13 |
TGF-β1, transforming growth factor-β1.
Association between serum levels of lncRNA-NEF and clinicopathological data of patients.
Variable | Nο. | High-expression | Low-expression | χ2 | P-value |
---|---|---|---|---|---|
Sex | 0.64 | 0.2 | |||
Male | 35 | 15 | 20 | ||
Female | 27 | 16 | 11 | ||
Age (years) | 0.26 | 0.61 | |||
>45 | 28 | 13 | 15 | ||
<45 | 34 | 18 | 16 | ||
Primary tumor diameter (cm) | 1.19 | 0.55 | |||
>4 | 26 | 15 | 11 | ||
2–4 | 17 | 7 | 10 | ||
<2 | 19 | 9 | 10 | ||
Lymph node metastasis | 5.21 | 0.02 | |||
Yes | 27 | 18 | 9 | ||
No | 35 | 13 | 22 | ||
Smoking | 0.06 | 0.8 | |||
Yes | 31 | 15 | 16 | ||
No | 31 | 16 | 15 | ||
Drinking | 2.45 | 0.12 | |||
Yes | 38 | 16 | 22 | ||
No | 24 | 15 | 9 |
lncRNA-NEF, long non-coding RNA-neighboring enhancer of forkhead box A2.