Papillary thyroid carcinoma (PTC) is the most common type of thyroid cancer. Hydroxysteroid dehydrogenase like 2 (HSDL2) can regulate lipid metabolism and take part in cell proliferation. The purpose of the present study was to explore functional role of HSDL2 gene in PTC. The expression of HSDL2 protein in PTC tissues was estimated using immunohistochemistry analysis (IHC). HSDL2 mRNA level was detected through quantitative real-time polymerase chain reaction (qRT-PCR). Effects of HSDL2 gene on cell proliferation and apoptosis were assessed using the shRNA method for both in vitro and in vivo experiments. Potential target genes of HSDL2 were determined via bioinformatics analyses and Western blotting. HSDL2 was up-regulated in PTC tissues and cell lines compared with the controls (all P<0.05). Inhibiting HSDL expression could suppress PTC cell proliferation and cycle, and promote apoptosis in vitro. In vivo, the knockdown of HSDL2 gene could significantly suppress tumor growth (all P<0.05). Furthermore, AKT3, NFATc2 and PPP3CA genes might be potential targets of HSDL2 in PTC. HSDL2 expression was increased in PTC tissues and cells, which could promote tumor progression in vitro and in vivo.
Papillary thyroid carcinoma (PTC) is the most common subtype of thyroid cancer. Its incidence exhibits continual increases in recent decades worldwide . PTC is more frequently observed in individuals of 20–55 years, especially among females . Early diagnosis remains a great challenge in PTC, due to its asymptomatic nature at early stages. Fine needle aspiration biopsy (FNA) and ultrasound imaging are two commonly used methods for PTC diagnosis, which have relatively high accuracy [3,4]. Overall survival of PTC cases is significantly improved due to great advancements in therapeutic strategies, such as surgery, chemotherapy and radiotherapy . However, the recurrence rate of PTC remains high, gravely weakening the effects of PTC treatment. This condition could partially be explained by increases in incurable cases and by limited understanding on the malignancy-related biological behaviors [6,7]. Therefore, exploring molecular mechanisms of PTC progression is critical to determine therapeutic targets for this malignant disease.
Short-chain dehydrogenases/reductases (SDRs) superfamily contains a series of crucial oxidoreductases . The family plays important roles in catalyzing the oxidation and reduction of various substrates, such as steroids, sugars, retinoids and fatty acids. Previous data have indicated that SDR enzyme dysfunction may influence metabolism, neural development, transformation, thus leading to diseases, such as obesity-related medical conditions, Alzheimer’s disease and cancers [9–11]. As a member of SDRs family, hydroxysteroid dehydrogenase like 2 (HSDL2) consists of a C-terminal SCP2-like domain and an N-terminal SDR domain . HSDL2 has been identified as an effective fatty acid regulatory factor in lipid metabolism . Lipid metabolism is an established hallmark in various human cancers [14–16]. For examples, the study by Hosokawa et al.  demonstrated that altered lipid metabolism was correlated with malignant transformation. The level of phosphatidylcholine (32:1) could be employed as a biomarker for the recurrence of triple-negative breast cancer . Lipids could provide energy for membrane formation and realize other functions for aggressively proliferating tumor cells . Additionally, lipid metabolism may play important roles in the activation of essential cell-signaling pathways in carcinogenesis, thus contributing to primary tumor initiation and distant metastasis . As an important regulator for lipid metabolism, HSDL2 has also been proved to participant in tumorigenesis. It was reported that HSDL2 could mediate cell proliferation and tumor growth in glioma via Akt-associated signaling pathway. The expression pattern of HSDL2 was positively correlated with aggressive progression of glioma . However, the study carried out by Zhang et al.  reported that overexpression of HSDL2 resulted in tumor suppressive effects on progression of cholangiocarcinoma via inhibiting cell growth and promoting cell apoptosis. HSDL2 might play diverse roles in different types of cancer. However, the effects of HSDL2 on PTC were rarely reported in the past.
In the present study, we aimed to investigate the expression patterns of HSDL2 gene in PTC tissues and cell lines, as well as its functional roles in PTC progression.
Methods and materials
Patients and tissue sample collection
PTC tissues and adjacent normal ones were collected from 17 patients, who were pathologically diagnosed with PTC at Affiliated Hospital of the Academy of Military Medical Sciences. None of the patients had received any anti-tumor therapies prior to the sampling. After the collection, the tissues were immediately stored in liquid nitrogen, and then kept at −80°C for further use. Experimental procedures were accomplished in accordance with the guidelines released by the Ethics Committee of Affiliated Hospital of the Academy of Military Medical Sciences. Signed written informed consent was obtained from each patient.
Cell culture and transfection
The cells K1 and Nthy-ori 3-1 were purchased from European Collection of Authenticated Cell Cultures (ECACC), while B-CPAP was purchased from the Stem Cell Bank, Chinese Academy of Sciences. Two PTC cell lines (K1: ECACC 92030501 and B-CPAP: SCSP (stem cell storage platform) 543) and human thyroid follicular epithelial cell line (Nthy-ori 3-1: ECACC 90011609) were used for subsequent cell experiments. These cell lines were cultured in RPMI-1640 medium containing 10% fetal bovine serum (FBS) (Gibco, Gaithersburg, U.S.A.). Cell cultures were incubated in a humidified chamber with 5% CO2 at 37°C. Cell morphology was performed for further identification of these cells.
Lentiviral vector GV115 carrying shRNA targeting HSDL2 (shHSDL2) was transferred into K1 and B-CPAP cell lines, so as to down-regulate HSDL2 expression. Corresponding empty GV115 vector (shCtrl) was used as negative control. Transfection was performed via Lipofectamine 2000 (Life Technologies, Carlsbad, CA, U.S.A.) following the instructions of the manufacturer. Transfection efficiency was estimated employing relative expression of HSDL2 mRNA in the transfected cells which was detected using quantitative real-time polymerase chain reaction (qRT-PCR).
Expression levels of HSDL2 protein in PTC and adjacent normal tissues were evaluated using immunohistochemistry analysis (IHC). The tissues were fixed by formaldehyde and embedded by paraffin. Then paraffin sections were deparaffinized in xylene and rehydrated in graded alcohols. In order to quench the activity of endogenous peroxidase, the sections were treated using 3% hydrogen peroxide. Later, the activities of antigens were recovered adopting citrate buffer (pH = 6.1) at 95°C for 15 min. The sections were blocked with normal goat serum at 37°C for 10 min, and then incubated with a polyclonal goat anti-HSDL2 antibody (diluted 1:200, Santa Cruz Biotechnology, CA, U.S.A.) overnight at 4°C. After rinsing with phosphate buffer solution (PBS), the sections were incubated with the second antibody (rabbit anti-goat antibody) at 37°C for 30 min. Last, the sections were incubated in the streptavidin–horseradish peroxidase complex. Staining results were reviewed and scored by two independent observers. Staining intensity was scaled as 0 (no staining), 1 (weak staining), 2 (moderate staining) and 3 (strong staining). The proportion of positively stained tumor cells was scored as 0 (0%), 1 (<25%), 2 (26–50%), 3 (51–75%) and 4 (>75%). Final score was calculated using staining intensity score and the proportion of positive tumor cells. Three fields were randomly selected under microscope for each specimen, and their average values were used for final analysis.
RNA extraction and qRT-PCR
Total RNA was extracted from PTC cell lines (K1 and B-CPAP) and from human normal thyroid cell line (Nthy-ori 3-1) using TRIzol reagent (Invitrogen, Carlsbad, CA, U.S.A.) according to the manufacturer’s instructions. RNA quality and concentration were determined using Nanodrop 2000 (Wilmington, DE 19810, U.S.A.) at the ratio of OD A260/A280. RNA would be adopted for subsequent analyses only when it had a ratio close to 2.0.
Reverse transcription-polymerase chain reaction (RT-PCR) was performed to synthesize cDNA from the obtained RNA using Transcriptor First Strand cDNA Synthesis Kit (Roche, Vilvoord, Brussels, Belgium). This process was as per the manufacturer’s protocols. qRT-PCR was conducted to evaluate relative expression level of HSDL2 mRNA using SYBR Green I Master Mix kit (Invitrogen, Carlsbad, CA, U.S.A.) on a 7300 Real-Time PCR System (Applied Biosystems, Foster City, CA, U.S.A.). GAPDH was used as the internal control gene. All of the primer sequences were as follows: HSDL2 5′-AAGCCACTCAAGCAATCTATCTG-3′ (forward) and 3′-GCTCTCCATATCCGACATTCCC-3′ (reverse); GAPDH 5′-TGACTTCAACAGCGACACCCA-3′ (forward) and 5′-CACCCTGTTGCTGTAGCCAAA-3′ (reverse). Final relative expression of HSDL2 mRNA was calculated with the 2−ΔΔCt method and normalized to GAPDH. Three separate cell culture samples were subjected to analysis in triplicate.
Cell viability assay
After the transfection, cell viability of the K1 and B-CPAP cell lines were detected with Celigo cell counting (Nexcelom Bioscience, Lawrence, MA, U.S.A.) and MTT assay. Logarithmic transfected cells were collected and digested using trypsin to obtain cell suspensions. The cell suspensions were seeded into a 96-well plate (2000 cells/well) and incubated in a humidified chamber with 5% CO2 at 37°C. The Celigo cell counting was performed once a day and lasted for 5 days. Cell number was recorded for the plotting of cell growth curve.
In MTT assay, cell suspensions were cultured in 96-well plates (1 × 104 cells/well) and incubated in a humidified chamber with 5% CO2 at 37°C. Each well was added with 20 µl MTT (5 mg/ml, Sigma) at the time points of 1, 2, 3, 4 and 5 days and continually cultured at 37°C for 4 h. Then the culture medium was removed and 100 µl DMSO (Sigma–Aldrich, St. Louis, Missouri, U.S.A.) was added into every well. Absorbance at 490 nm was measured for the cell cultures. Day 1 meant 24 h after transfection. The values for day 1 were recorded as 1, and relative fold changes at each time point were recorded. All of the cell experiments were performed in triplicate using three separate cell cultures.
Cell cycle and apoptosis assay
Cell cycle and apoptosis analyses of PTC cells were carried out using flow cytometry. K1 and B-CPAP cell lines after transfection were fixed with 75% ethanol for at least 1 h and washed using D-Hanks. Then the cells were stained with PI (Sigma–Aldrich, St. Louis, Missouri, U.S.A.) for 30 min. After the incubation at 4°C, the cells were detected using FACS Calibur flow cytometer (BD Biosciences, Franklin Lakes, NJ, U.S.A.). The obtained data were subsequently analyzed employing CellQuest software (BD Biosciences, Franklin Lakes, NJ, U.S.A.).
For the analysis on cell apoptosis, the apoptosis of the transfected cells were evaluated using Annexin V/propidium iodide detection kit (KeyGene, Nanjing, China) following the manufacturer’s instructions. FACS Calibur flow cytometer was used to detect the cells, and the data were analyzed using CellQuest software. Three separately prepared cell cultures were subjected to analysis in triplicate.
Nude mice xenograft assay
The stud9y procedures were approved by the Experimental Animal Ethics Committee of Affiliated Hospital of the Academy of Military Medical Sciences.
In pre-experiment, the tumorigenicity of K1 and B-CPAP were tested. The PTC cells which were infected with Lentiviral vector GV115 were mixed with Matrigel at the ratio of 1:1. The cells of 1E+7 were injected into nude mice at armpit through subcutaneous injection. A total of six nude mice for the pre-experiments were randomly divided into two groups (three in each group), treated with K1 and B-CPAP cells, respectively. Tumor formation and growth capacity were examined within 8 days after injection. Twenty-eight days after injection, the mice were killed, and tumors were then isolated. Tumor weights and sizes were detected to estimate the tumorigenicity of the cells, and the tumors with a volume of 100 mm3 were considered to have stable tumorigenicity. Only cells with stable and high tumorigenicity were used for subsequent analyses.
A total of 20 female BALB/c mice (4 weeks old, 18–20 g) were obtained from the Experimental Animal Center of Changchun Biological Institute (Changchun, China), and maintained under a specific pathogen-free condition with free access to water and food. The mice were randomly divided into two groups (ten mice in each group), namely HSDL2 knockdown group (KD) and negative control group (NC). Matched cell suspensions containing shHSDL2 or shCtrl were given to nude mice at their armpits through subcutaneous injection. Each mouse received 1E+07 cells. Tumor growth was observed once a day after the injection, and tumor volume was recorded as well. Ten animals were used for analysis, and each sample was subjected to triplicate analyses.
Twenty-eight days later, the whole-body imaging was conducted for the mice. All of the mice were killed, and their tumors were isolated. The weights and sizes of the tumors were measured, and then they were fixed in paraformaldehyde.
Potential target genes of HSDL2 gene
In order to inspect molecular mechanism of HSDL2 gene in PTC, potential target genes of HSDL2 were predicted according to bioinformatics analyses using the GeneChip® PrimeView™ Human Gene Expression Array (Affymetrix, Santa Clara, CA, U.S.A.). Gene expression array assay was carried out by Shanghai Genechem Co., Ltd. (Shanghai, China). Three separately cultured cell samples were subjected to triplicate analyses. K1 cells were transfected by shHSDL2 and shCtrl vectors, respectively. The transfected cells were incubated in a humidified chamber with 5% CO2 at 37°C for 72 h. Then, the cells were harvested for gene expression array assay. In brief, total RNA sample was extracted from transfected K1 cells using TRIzol reagent (Invitrogen, Carlsbad, CA, U.S.A.) according to the manufacturer’s instructions. After purification, total RNA was used to prepare amplified RNA using GeneChip 3′IVT Express Kit (Affymetrix, Santa Clara, CA, U.S.A.). The amplified RNA was purified and fragmented for hybridization on gene expression array. Then raw data were analyzed using Partek® Genomics Suite (Partek Incorporated, St. Louis, U.S.A.), and P-values less than 0.05 were considered significant. Genes with a fold change more than 3 were chosen for pathway analysis using IPA software (www.ingenuity.com). IPA, an integrated online analysis software, can help understand gene expression data, microRNA data and small-scale experimental data. The software establishes a visualized experimental system that could construct interaction network between gene, protein as well as chemicals and drugs.
Then identified target genes were verified in PTC tissue specimens collected from all of the nude mouse models (ten mice in each group) using Western blotting. In KD group, proteins were extracted from PTC tissue specimens collected from ten mice, and mixed protein specimens were used for subsequent analysis. Same operations were performed for NC group. Each sample was subjected to triplicate analyses.
Transfected cells were collected and lysed with 2× Lysis Buffer (Sigma–Aldrich, St. Louis, Missouri, U.S.A.). Total proteins in the cell or tissue samples were quantitated using BCA protein assay kit (Pierce Biotechnology, Rockford, IL, U.S.A.) following the instructions. The obtained proteins were first separated using 10% SDS/PAGE and then transferred on to polyvinylidene fluoride membranes (PVDF, Invitrogen, Carlsbad, CA). The membranes were blocked using TBST solution which was supplemented with 5% skim milk at 4°C for 1 h, and then incubated with first antibodies against AKT3 (1:1000, CST#9272, Boston, U.S.A.), NFATc2 (1:500, Abcam ab2722, Cambridge, U.K.), PPP3CA (1:2000, Abcam ab3673, Cambridge, U.K.), FOS (1:200, Abcam ab7963, Cambridge, U.K.) and AKT1S1 (1:1000, CST#2691, Boston, U.S.A.) overnight at 4°C, followed by the incubation with second antibodies for 1.5 h at room temperature. The blots were visualized with enhanced chemiluminescence kit (GE Healthcare, Chalfont St. Giles, Buckinghamshire, U.K.) following the manufacturer’s protocols.
All statistical analyses were performed using SPSS 18.0 software (SPSS Inc., Chicago, IL, U.S.A.). All experiments were carried out in triplicate. Quantitative variables were expressed as mean ± SD, and examined through one-way ANOVA test among multiple groups. Comparisons on quantitative data between the two groups were carried out using Student’s t test. Differences were considered statistically significant when P<0.05.
Baseline characteristics of PTC patients
A total of 17 PTC patients including 6 males and 11 females were collected in our study. Their average age was 48.75 ± 8.62 years. Of them, 3 (17.65%) had tumor size more than 2 cm, and 10 (58.82%) had unilateral tumor. According to TNM staging, 13 (76.47%) patients were classified into I/II stages while 4 (23.53%) into III/IV stages. The basic characteristics of the patients are summarized in Table 1.
|Characteristics .||Number of patients .|
|Average age (years)||48.75 ± 8.62|
|Tumor size, cm|
|TNM stage (AJCC)|
|Characteristics .||Number of patients .|
|Average age (years)||48.75 ± 8.62|
|Tumor size, cm|
|TNM stage (AJCC)|
Up-regulated HSDL2 expression in PTC tissues and cell lines
Representative IHC results for HSDL2 in adjacent normal tissues and PTC ones are shown in Figure 1A,B, respectively. Mean expression score of HSDL2 protein was 0.50 ± 1.27 in adjacent normal tissues and 8.05 ± 4.71 in PTC ones, indicating that the expression level of HSDL2 was significantly higher in PTC tissues than in adjacent normal ones (Figure 1C, P<0.01).
Expression of HSDL2 protein was measured using IHC for tissue specimens collected from PTC patients
HSDL2 mRNA expression and protein level in PTC cell lines (K1 and B-CPAP cells) and in human normal thyroid cell line (Nthy-ori 3-1) were also assessed. The cells were detected through cell morphology under microscope. Figure 2A,B show representative characteristics of K1 cell clone under inverted microscope. The cell clones possessed spindle or typical epidermal cell characteristics, and were arranged closely. Only cell clones with typical morphologic parameters were used for subsequent analysis. The level of HSDL2 protein was obviously increased in PTC cell lines, compared with Nthy-ori 3-1 cell line (Figure 2C). Relative expression of HSDL2 mRNA was remarkably higher in K1 and B-CPAP cells than in normal cells (all P<0.05, Figure 2D).
Expression pattern of HSDL2 in PTC cell lines
Knockdown of HSDL2 gene suppressed the proliferation of PTC cells
In order to examine functional role of HSDL2 gene in PTC, the gene was silenced using shHSDL2 in K1 cells and B-CPAP cells. After the transfection, relative expression levels of HSDL2 mRNA were measured via qRT-PCR (Figure 3A,B). The results suggested that the levels of HSDL2 in transfected cells were significantly decreased, revealing good transfection efficiency. Celigo cell counting and MTT assay were performed to explore the effect of HSDL2 on cell proliferation. Celigo test results indicated that the numbers of both K1 and B-CPAP cells were decreased in shHSDL2 group when compared with shCtrl group (all P<0.05, Figure 3C–F). Besides, MTT results shown in Figure 3G,H indicated that the knockdown of HSDL2 gene could significantly suppress cell proliferation both in K1 and B-CPAP cells, compared with control groups (all P<0.05). Meanwhile, we conducted the rescue experiences though the transfection of LV-HSDL2 for overexpression in shHSDL2 transfected cells. The final results showed that overexpression of HSDL2 in HSDL2 silencing cells could significantly increased the proliferation of PTC cells (P<0.05) and reversed the effect of shHSDL2 on PTC cells.
Knockdown of HSDL2 gene suppressed the proliferation of PTC cells
Knockdown of HSDL2 gene induced cell cycle disorder and increased the apoptosis of PTC cells
Results from cell cycle analysis suggested that decreased HSDL2 expression in both K1 and B-CPAP cells significantly reduced G1 period and increased S period (all P<0.05, Figure 4A,B). As shown in Figure 4C,D, the apoptosis percentages of K1 and B-CPAP cells were elevated in shHSDL2 group, compared with shCtrl group (all P<0.01) (Supplementary Figure S1).
Effects of HSDL2 gene on cell cycle and apoptosis of PTC cells
Reduced HSDL2 expression inhibited PTC cell tumorigenicity in vivo
In our pre-experiment, the tumorigenicity of K1 and B-CPAP cells were tested. In K1 group, tumor formation was obvious in three nude mice 14 days after injection, and their tumor volumes were more than 100 mm3 28 days after injection, suggesting tumorigenicity was moderate (Figure 5A). And K1 cells could be used for subsequent analysis. In B-CPAP group, tumor appeared in three mice after 15–20 days, suggesting weak tumorigenicity of B-CPAP cells. Moreover, the tumor volumes in these mice were less than 100 mm3 (Figure 5B). All if the data suggested that B-CPAP cells might be not suitable for animal experiments, and only K1 cells were chosen for subsequent analysis.
Tumor size detection in pre-experiments at day 28 after injection
K1 cells stably transfected with shHSDL2 (KD group) or shCtrl (NC group) were implanted into nude mice for tumor formation. As shown in Figure 6A, tumor volume was significantly less in KD group (injected with the K1 cells transfected with shHSDL2) than in NC group in the first 8 days (P<0.05 for all). At day 28 after injection, tumor weights and sizes were estimated for nude mice in each group. As shown in Figure 6B,C, inhibiting the expression of HSDL2 gene could obviously reduce tumor weights and sizes in animal models (P<0.05).
HSDL2 knockdown inhibited PTC tumorigenicity in vivo
To further confirm these results, whole-body imaging was obtained for the treated mice. As shown in Figure 7, fluorescent expression was remarkably lower in KD group than in NC group (P<0.05).
Whole-body imaging in nude mice xenograft assay
AKT3, NFATc2 and PPP3CA were potential targets of HSDL2 in PTC
Human Gene Expression Array (Affymetrix, Santa Clara, CA, U.S.A.) presented a gene interaction network for molecular mechanism of HSDL2 knockdown in K1 cell lines (Figure 8). From the figure we saw that the down-regulation of HSDL2 gene could enhance the expression of AKT1S1 and FOS while inhibit the expression of AKT3, NFATc2 and PPP3CA.
Gene interaction network obtained via bioinformatic analyses for HSDL2 gene knockdown in K1 cell line
Major downstream genes (AKT1S1, AKT3, FOS, NFATc2 and PPP3CA) of HSDL2 in the network were checked with Western blotting in tissue specimens collected from the nude mice (ten samples from each group). Analysis results indicated that AKT3, NFATc2 and PPP3CA protein expressions were significantly lower in KD group than in NC group (all P<0.05, Figure 9).
Expressions of downstream genes of HSDL2 in mouse models
As the most common type of thyroid cancers, PTC has received more and more attention because of its increasing morbidity and mortality worldwide. Benefited from considerable advancements in therapeutic technologies, PTC prognosis and outcomes witness significant improvements [21,22]. However, some PTC patients, approximately 10% of all the cases, are incurable due to metastasis and relative high tumor recurrence . Therefore, it is critical to explore molecular mechanisms underlying PTC progression.
In previous studies, numerous cancer-related genes have been identified to be closely correlated with PTC progression [24–27]. For example, microRNA-126 was found to be down-regulated in PTC tissues and cell lines, while its up-regulation could suppress cell proliferation, migration and invasion, and promote the apoptosis of PTC cells . Up-regulated expression of lysine-specific demethylase 1 (LSD1) has been detected in PTC cells, and its knockdown inhibited cell proliferation, tumorigenicity and invasion . The growth and migration of PTC cells have been enhanced by the overexpression of hematopoietic pre-B cell leukemia transcription factor (PBX)-interacting protein (HPIP) . In addition, Di Maro et al.  found positive relationship for elevated expression of anterior gradient protein 2 (AGR2) with increased migration and invasion capacity of PTC cells, which predicted poor overall survival of the patients. All these researches indicated the importance of genes in cancer development.
HSDL2 belongs to SDR superfamily which exerts important influences on the metabolism of sugars, retinoids, steroids, xenobiotics and fatty acids . Evidences have shown that HSDL2 played a potential role in lipid metabolism [33,34]. Lipid metabolism is an important event in tumor development, and has been reported to be elevated in some cancer cells. Thus, it is reasonable to hypothesize that HSDL2 might be involved in tumor progression. HSDL2 up-regulation has been observed in human glioma samples, and reported to have close relationship with tumor proliferation, cell cycle and apoptosis . However, the role of HSDL2 in PTC remains poorly known until now. In the present study, we investigated the expression patterns of HSDL2 gene and protein in both PTC tissues and cell lines, as well as its functional role in PTC development.
In our research, HSDL2 protein level was higher in PTC tissues than in adjacent normal ones. Similarly, evaluated expressions of HSDL2 mRNA and protein were also observed in two PTC cell lines, compared with normal human thyroid follicular epithelial cell line. All of these results suggested an oncogenic role of HSDL2 gene in PTC. In order to testify such effect, we inhibited HSDL2 expression in PTC cell lines via Lentiviral vector transfection. And the knockdown HSDL2 expression significantly decreased cell proliferation, and induced cell apoptosis in both K1 and B-CPAP cell lines. Furthermore, mice injected with HSDL2-knockdown K1 cells had smaller tumor size, volume and weight than those receiving shCtrl. All of these data suggested that as an oncogene, HSDL2 could promote PTC progression. Inhibiting HSDL2 expression might suppress aggressive behaviors of PTC cells, as well as its malignant progression. So HSDL2 might be a potential therapeutic target for PTC. Such conclusion was in line with the results obtained in the study on glioma by Ruokun et al. . It is worthy to note that B-CPAP cells also presented high expression of HSDL2, but their tumorigenicity in vivo was much low. The observation might imply that oncogenic mechanisms of PTC may be not induced merely by a single gene. Tumor promoting pathway induced by HSDL2 in B-CPAP cells might be inhibited. The functions of HSDL2 in PTC might be distinct in different types of tumor cells. Therefore, it is urgent to explore molecular mechanisms of HSDL2 in PTC.
Bioinformatics analyses suggested that various genes were involved in the interaction network of tumor-promoting role of HSDL2 gene in PTC. The knockdown of HSDL2 gene in PTC could induce the down-regulations of AKT3, NFATc2 and PPP3CA proteins. And their corresponding genes were confirmed as candidate targets for HSDL2 gene in PTC. HSDL2 could promote aggressive progression of PTC via mediating the expression of AKT3, NFATc2 and PPP3CA. AKT3, a member of AKT family, is involved in the regulations of various cellular processes, such as cell proliferation, migration, invasion and apoptosis. Its overexpression was observed in a variety of human cancers, including prostate cancer, glioma and PTC [35–37]. Reportedly, AKT3 up-regulation contributed to malignant progression in PTC . Moreover, the study carried out in glioma demonstrated that HSDL2 might regulate tumor progression through AKT-associated signaling pathway . In the current study, we found that HSDL2 knockdown weakened the expression of AKT3, suggesting that the oncogenic function of HSDL2 in PTC might be correlated with AKT signaling pathways. NFATc2 is a calcium-responsive parlor, and potentially promotes cell invasion, migration, survival and angiogensis . While PPP3CA protein is responsible for maintaining intracellular calcium homeostasis . Alterations in these two proteins might contribute to malignant transformation of human cells, thus leading to tumors. Inhibiting HSDL2 expression in PTC could decrease NFATc2 and PPP3CA, suggesting functional roles of HSDL2 in PTC might implicate NFATc2 and PPP3CA proteins. However, it is worth noting that in gene expression microarray assay for K1 cells, the cell lines, showing similar characteristics as several other types of cancer cell lines, gradually lost some original properties. Thus, some PTC-specific genes targeted by HSDL2 might be misdetected. The microarray analysis should be verified in original PTC cell line obtained from PTC tissues. In addition, BRAF (V600E) mutation, frequently observed in PTC, may influence the development and progression of PTC . Besides, BRAF mutation may also affect gene expression in PTC cases [41,42]. In our study, K1 cells exert BRAF mutation, the tumor-promoting role of HSDL2 gene, or its interaction network in PTC presenting BRAF-wt remained poorly known. The association between HSDL2 and BRAF genes is rarely explored, but studies are still necessary to explore molecular mechanisms underlying the functional roles of HSDL2 in BRAF wild PTC.
The present study preliminarily investigated the functional roles of HSDL2 gene in PTC, as well as the related mechanisms. Despite the encouraging results, there were still several limitations in the present study. First, the sample size was relatively small. Second, we found that the expression levels of HSDL2 in PTC tissue and cell specimens were significantly increased, and that HSDL2 knockdown could inhibit tumor growth. However, whether its overexpression in normal cells could induce tumorigenesis remained obscure. Moreover, Sun et al.  reported that HSDL2 could also contribute to cell motility of ovarian cancer, revealing its promoting effects on tumor metastasis. Whether HSDL2 was involved in early metastasis of PTC required further investigation. Third, although growing evidences have demonstrated that HSDL2 gene could influence lipid metabolism, such effect was not detected in our study. Whether HSDL2 regulated PTC progression via its function on lipid metabolism remained unclear. Fourth, microarray expression analysis was only performed in cell experiments, and verified in PTC tissues obtained from animal models in our study. Some potential target genes might be missed. Further microarray expression analyses in in vivo model are necessary to improve our findings. In addition, exact molecular mechanisms underlying regulatory effects of HSDL2 on AKT3, NFATc2 and PPP3CA expressions remained unclear, and so did the question that whether HSDL2 mediated aggressive progression of PTC via regulating their expressions. Further researches will be needed to explore related molecular mechanisms. Therefore, well-designed studies with larger sample size are required to verify our observations.
In conclusion, HSDL2 expression was significantly up-regulated in PTC tissues and cells. Knockdown of HSDL2 gene could suppress cell proliferation and promote cell apoptosis for PTC cells, thus inhibiting tumor growth in vivo. Functional roles of HSDL2 gene in PTC might be associated with AKT3, NFATc2 and PPP3CA genes. HSDL2 promoted PTC progression which could be employed as a novel therapeutic target for the cancer. The present study may be the first investigation to explore the expression pattern and function of HSDL2 in PTC.
The present study was supported by the Ethics Committee of the Affiliated Hospital of the Academy of Military Medical Sciences and also has been carried out in accordance with the World Medical Association Declaration of Helsinki.
The subjects had been informed the objective. Certainly, written consents were signed by every subject in the present study.
Jing Zeng and Yi Fang conceived and designed the experiments. Xiao Ma, Jinjing Wang and Ran Liu analyzed the data. Yun Shao, Yanwei Hou and Zhiyuan Li wrote the paper. Jing Zeng, Xiao Ma and Jinjing Wang performed the experiments. All authors read and approved the final manuscript.
The authors declare that there are no sources of funding to be acknowledged.
The authors declare that there are no competing interests associated with the manuscript.
American Joint Committee on Cancer
European Collection of Authenticated Cell Cultures
hydroxysteroid dehydrogenase like 2
Ingenuity Pathway Analysis
nuclear factor of activated T cells c2
protein phosphatase 3 catalytic subunit a
papillary thyroid carcinoma
quantitative real-time polymerase chain reaction
Sterol carrier protein 2
Tris-buffered saline containing Tween-20
Tumor Node Metastasis