- Open Access
IGFBP7 inhibits cell proliferation by suppressing AKT activity and cell cycle progression in thyroid carcinoma
- Le Zhang†1, 2,
- Rong Lian†1, 2,
- Jingjing Zhao3, 4,
- Xianming Feng1, 2,
- Runyi Ye5,
- Lingxiao Pan6,
- Jueheng Wu1, 2,
- Mengfeng Li1, 2,
- Yongbo Huan7Email author and
- Junchao Cai1Email author
© The Author(s) 2019
- Received: 30 March 2019
- Accepted: 1 June 2019
- Published: 6 June 2019
Thyroid cancer is the most common malignant endocrine tumor and is classified into papillary thyroid cancer (PTC), follicular thyroid cancer (FTC) and anaplastic thyroid cancer (ATC), which have substantially different characteristics. Insulin-like growth factor binding protein 7 (IGFBP7) has recently been recognized as a tumor suppressor in many cancer types. However, the expression pattern of IGFBP7 and its biological function in various types of thyroid carcinoma remain poorly understood.
We found that the protein levels of IGFBP7 in FTC and ATC tissues were significantly lower or even absent compared with those in normal thyroid, benign thyroid adenoma and classical PTC tissues. Moreover, overexpression of IGFBP7 in two undifferentiated ATC cell lines, ARO and FRO, and one differentiated FTC cell line, WRO, significantly inhibited cell proliferation in vitro. In vivo experiments revealed that ectopic IGFBP7 expression markedly suppressed growth of tumor xenografts derived from these thyroid cancer cell lines, while IGFBP7 silencing accelerated tumor growth. At the mechanistic level, overexpression of IGFBP7 dramatically suppressed phosphorylation-mediated activation and kinase activity of AKT, causing an upregulation of cyclin-dependent kinase (CDK) inhibitors p27Kip1 and p21Cip1 and induction of G1/S cell cycle arrest, while silencing IGFBP7 exerted the opposite effects.
IGFBP7 expression is decreased or even absent in FTC and ATC. Acting as a cell cycle repressor, IGFBP7 plays an important tumor-suppressive role in human thyroid cancer, especially in FTC and ATC subtypes and may represent a promising biomarker and therapeutic target for human thyroid cancer treatment.
- Thyroid cancer
- Cell cycle
Thyroid cancer is the most common malignant endocrine tumor. The incidence of thyroid cancer is rapidly increasing worldwide and annually increasing in China, mainly due to improvements in thyroid cancer diagnostic technologies, especially increased detection of thyroid microcarcinoma . According to data from the National Cancer Institute, thyroid cancer is responsible for 567,000 cancer cases worldwide, ranking ninth in tumor incidence. The global incidence rate of 10.2 per 100,000 in women is 3 times higher than that in men. Thyroid cancer accounts for 5.1% of the total estimated cancer burden in females in 2018 . Most thyroid cancer cases originate in the follicular epithelium and can be divided into papillary thyroid cancer (PTC), follicular thyroid cancer (FTC) and anaplastic thyroid cancer (ATC) according to the pathologic types. Among all thyroid cancer cases, over 80% are PTC, which is common in young women and children, and FTC and ATC accounts for only 15% and less than 5% of cases, respectively . Differentiated thyroid carcinoma (DTC), including PTC and FTC, has a favorable prognosis due to slow growth, well differentiation and low-grade malignancy. However, approximately 20–30% of PTC patients will develop recurrence, and patients with recurrent disease have poor prognoses. Notably, in contrast, ATC is characterized by poor differentiation and is notorious for its aggressive clinical behavior and tendency to rapidly metastasize and develop intrinsic resistance to chemotherapy, making it one of the most malignant tumors . Even with aggressive therapy, the 5-year survival rate of ATC patients is less than 10%. Due to the lack of effective biomarkers for well-differentiated and poorly differentiated thyroid carcinoma, inappropriate excessive treatments have been used in clinical therapy. Therefore, there is an urgent need to investigate the molecular mechanisms underlying the development and progression of thyroid cancer for identifying potential molecular biomarkers to distinguish various subtypes of thyroid cancer and develop effective therapeutic strategies.
The insulin-like growth factor (IGF) signaling pathway is important for regulating cell proliferation, differentiation and apoptosis in mammals and for promoting tumor development and progression. Insulin-like growth factor binding proteins (IGFBPs) affect the interaction between IGF and its receptor and regulate the activity of the IGF signaling pathway. The IGFBP family consists of seven structurally homologous proteins (IGFBP1–IGFBP7), which bind insulin-like growth factor I (IGF-I) and insulin-like growth factor 2 (IGF-II) with high affinity, carry and transfer these IGFs, and extend their half-lives, thus regulating the biological function of IGFs. Among the IGFBPs, IGFBP7, a soluble protein identified in normal meningeal cells and mammary epithelium cells in humans, has been found to bind IGFs with low affinity and to bind insulin with high affinity. In addition, IGFBP7 can participate in a variety of pathophysiological processes, such as cell growth, differentiation, development, senescence and carcinogenesis, independent of the IGF signaling pathway. IGFBP7 is highly expressed in senescent breast epithelial cells . Accumulating evidence suggests that IGFBP7 serves as a tumor suppressor in various types of cancers. Downregulation and even deletion of IGFBP7 have been found in breast cancer, lung cancer, bladder cancer, colorectal cancer, prostate cancer and melanoma, and low levels of IGFBP7 in tumor tissues are correlated with poor prognosis [6–10]. Overexpression of IGFBP7 in lung cancer cells inhibits anchorage-independent growth and xenograft tumor growth . Similar findings have been obtained in other cancer types, such as colon cancer, prostate cancer and melanoma [12–14]. However, the expression pattern of IGFBP7 and its biological function in various types of thyroid carcinoma have not been clearly elucidated.
In this study, we found that IGFBP7 expression is greatly decreased and even absent in follicular and anaplastic thyroid carcinoma compared to that in normal thyroid tissue, adenoma and classical PTC. Overexpression of IGFBP7 in two undifferentiated human anaplastic thyroid carcinoma cell lines, ARO and FRO, and one differentiated follicular human thyroid carcinoma cell line, WRO, significantly inhibits tumor proliferation both in vitro and in vivo, whereas knockdown of endogenous IGFBP7 in WRO cells substantially increases proliferation and tumor growth. Furthermore, IGFBP7 dramatically suppresses the phosphorylation-mediated activation and kinase activity of AKT, causing upregulation of cyclin-dependent kinase (CDK) inhibitors, p27Kip1 and p21Cip1, and induction of G1/S cell cycle arrest. Taken together, our findings suggest that IGFBP7 plays an important tumor-suppressive role in human thyroid cancer, especially in FTC and ATC subtypes and may represent a promising biomarker and therapeutic target for the disease.
IGFBP7 expression is downregulated in the FTC and ATC subtypes of thyroid cancer
IGFBP7 inhibits the proliferation of thyroid cancer cells in vitro
IGFBP7 suppresses tumor growth of thyroid cancer cells in vivo
IGFBP7 induces the expression of the cell- cycle inhibitors p21Cip1 and p27Kip1, leading to cell cycle arrest
IGFBP7 suppresses the phosphorylation-mediated activation and kinase activity of AKT in thyroid cancer
Thyroid cancer is the most commonly diagnosed endocrine malignancy. Thyroid cancer is an excellent example of how technological advancements in diagnostic imaging have led to the detection of indolent disease. Although an increase in incidence is largely confined to the more indolent histological subtype and to early tumor stages, thyroid cancer is a disease with several diverse subtypes. The various subtypes, mainly PTC, FTC and ATC, are different in their unique biology, natural history, prognosis, and available therapeutic options [15–20]. Although PTC patients have a favorable prognosis, approximately 20–30% of PTC patients will develop recurrence and recurrent diseases have poor therapeutic responsiveness similar to undifferentiated thyroid carcinomas [21–23]. Molecular studies are being focused on better characterizing the various subtypes of thyroid cancer and improving diagnosis by fine-needle aspiration biopsy. However, definite markers for the different subtypes of thyroid cancer are yet to be identified. Thyroid cancer pathology has generally been limited to the identification of features that predict aggressiveness, within the accepted “malignant” categories of PTC, ATC and FTC. Notably, our current study demonstrated that the expression of IGFBP7 in FTC and ATC is significantly lower or even absent compared with that in normal thyroid tissues, benign thyroid tumors and PTC. Furthermore, CPTC shows strong immunostaining for IGFBP7, whereas FVPTC hardly shows detectable levels of IGFBP7. These data suggest that IGFBP7 may be a valuable biomarker for FTC and ATC, both of which have malignant features. Similarly, IGFBP7 is almost undetectable in ATC cell lines and moderately expressed in FTC cell lines. Moreover, overexpression of IGFBP7 potently suppresses, and silencing of IGFBP7 accelerates proliferation and tumor growth of both ATC and FTC cell lines, suggesting the important role for the loss of IGFBP7 expression during thyroid cancer development and progression. Notably, many newly diagnosed cases of thyroid cancer present only as microcancerous lesions, making it difficult to discern the histological types and to choose appropriate treatment . Since IGFBP7 is a secretory protein that could be easily detected in clinical specimens such as blood, it is of great interest to detect levels of serum IGFBP7 in patients with benign thyroid adenoma or malignant thyroid carcinoma of various subtypes, such that serum IGFBP7 levels might be used as valuable biomarkers for the early diagnosis and clinical therapy of thyroid neoplasms.
Different types of thyroid cancer have unique gene mutations, suggesting that different molecular mechanisms may be related to the development and progression of thyroid cancer. Point mutations in the BRAF or RAS gene or RET/PTC rearrangements, all of which lead to constitutive activation of the mitogen-activated protein kinase (MAPK) signaling pathway, can be found in approximately 70% of thyroid cancer patients. Nevertheless, it is not common to have two or more mutations in the same patient at the same time [25, 26]. Among these mutations, BRAFV600E is considered to be the marker for the diagnosis and prognosis of papillary thyroid cancer and is closely related to extrathyroidal infiltration, lymph node metastasis, clinical stage, recurrence and mortality of thyroid cancer . It has been reported that IGFBP7 inhibits the BRAF-MEK-ERK pathway in an autocrine or paracrine manner and causes apoptosis in BRAF mutation-positive melanoma cells. However, we detected the phosphorylated levels of MEK and ERK in thyroid cancer cells with overexpression or knockdown of IGFBP7 and found that IGFBP7 did not impact on the BRAF-MEK-ERK pathway (data not shown). In parallel, the various thyroid cancer tissues collected in our study showed loss of IGFBP7 expression regardless of BRAF status. In fact, an increasing number of studies suggest that hyperactivation of the PI3K/AKT signaling pathway is as important as the BRAF-MEK-ERK pathway during tumor development and progression. For example, Maria et al. demonstrated that the PI3K/AKT signaling pathway is activated in more than 50% of thyroid cancer cases . Several reports have shown that gene mutations in the PI3K/AKT pathway are mainly present in poorly differentiated thyroid cancer tissues [29–31], suggesting that the activation of the PI3K/AKT signaling pathway may play an important role in the development and progression of thyroid cancer. In support of this notion, our current study reveals that IGFBP7 potently suppresses the growth of ATC and FTC cell-derived tumors and inhibits both phosphorylation-mediated activation and kinase activity of AKT. Therefore, our data suggest that the loss of IGFBP7 causes overactivation of the AKT signaling pathway, an effect essentially equivalent to that of the well-documented genetic mutations causing overactivation of the BRAF-MEK-ERK pathway. Notably, as IGFBP7 is a secreted protein and has low affinity for IGF, how IGFBP7 blocks the activation of AKT signaling remains to be investigated.
From a biological point of view, tumors, characterized by hyperproliferation, disrupted cell cycle and dysregulated of signal transduction pathways, are indicative of progressive disorders in cell cycle regulation. In normal cells, each stage of the cell cycle is controlled by a series of regulatory mechanisms to ensure that the cell cycle is carried out in a strict and orderly fashion. Three key classes of regulatory molecules, namely, cyclins, cyclin-dependent kinases (CDKs) and cyclin-dependent kinase inhibitors (CKIs), determine the progress of a cell through the cell cycle. Therefore, it is important to determine which types of these regulatory molecules are involved under a certain condition. In this study, we found that ectopic expression of IGFBP7 dramatically upregulates the levels of p27Kip1 and p21Cip1 and that the silencing of IGFBP7 causes the opposite effects in ATC and FTC cells. Notably, the cell cycle regulator p27Kip1 is a tumor-suppressive protein that broadly inhibits CDKs and plays an important role in resting cells in the G1 phase during the cell cycle . P21Cip1 which halts the cell cycle in the G1 phase by binding to and inactivating cyclin-CDK complexes is also a negative regulator of cell cycle progression and a typical tumor suppressor gene . After the inhibition of protein kinase activity in cyclin-CDK complexes by p27Kip1 and p21Cip1, Rb is in a state of hypophosphorylation. Hypophosphorylated Rb can bind the critical transcription factor E2F, making it lose its function and causing cell cycle arrest at G1 phase . Indeed, our data demonstrate that IGFBP7 overexpression significantly increases the percentage of cells in the G0/G1 phase and reduces the percentage of cells in the S phase of the cell cycle, and IGFBP7 silencing causes the opposite effects in ATC and FTC cells. Thus, we propose that IGFBP7 induces G1-S phase arrest during the cell cycle by upregulating the expression of two critical CKIs, namely, p27Kip1 and p21Cip1, to potently inhibit the proliferation of ATC and FTC cells. Notably, the AKT signaling pathway has been widely reported to decrease the expression of p27Kip1 and p21Cip1 through inactivating its downstream substrates, such as FOXO transcriptional factors, and to promote cell cycle progression [35–39]. Therefore, whether and how IGFBP7 inhibits the AKT signaling pathway to upregulate the expression of p27Kip1 and p21Cip1 in thyroid cancer requires further investigation.
Although IGFBP7 is present in almost all normal tissues, IGFBP7 is downregulated or even absent in a variety of tumor types, including breast cancer, lung cancer, bladder cancer, colorectal cancer, prostate cancer, melanoma and thyroid cancers [40–42]. Similar to that for many other tumor suppressors, the downregulated expression of IGFBP7 in tumor tissues is mainly ascribed to genetic and epigenetic regulation. It was reported that loss of heterozygosity (LOH) causes loss of expression of IGFBP7 in breast cancer . Accumulating evidence has demonstrated that hypermethylation of the IGFBP7 gene promoter leads to its loss of expression. Moreover, tumor cells lacking IGFBP7 expression could be restored by treatment with the DNA methylation inhibitor 5-aza-2′-deoxycytidine [7, 43]. Therefore, it is of great interest to further investigate whether the significant downregulation of IGFBP7 in ATC and FTC tissues, but not in classical PTC tissues, is caused by LOH or hypermethylation.
Taken together, results from the present study showed that the expression of IGFBP7 is significantly downregulated and even absent in thyroid follicular carcinoma and anaplastic carcinoma tissues. IGFBP7 might act as a tumor suppressor by inhibiting the proliferation of thyroid cancer cells via the downregulation of the activity of AKT, leading to an increase in the expression of the cell cycle inhibitors p27Kip1 and p21Cip1.
This study was conducted with a cohort of paraffin-embedded sections of 112 thyroid tumor patients, who had undergone surgical resection in the first affiliated hospital of Sun Yat-sen university during the period of 2005 to 2010. The histologic types of the above tumor samples were as the following: 18 cases of thyroid adenomas, 63 cases of papillary thyroid cancer, 15 cases of follicular thyroid cancer, 16 cases of anaplastic thyroid cancer.
The undifferentiated thyroid cancer cell lines FRO and ARO, follicular thyroid cancer cell lines WRO were gifted from the surgical laboratory of the Chinese University of Hong Kong, and maintained in DMEM medium (Invitrogen, Carlsbad, CA) supplemented with 10% fetal bovine serum (HyClone, Logan, UT) and 1% penicillin/streptomycin (Invitrogen, Carlsbad, CA), according to the protocols of previous reports . All cell lines were authenticated by short tandem repeat fingerprinting at Medicine Laboratory of Forensic Medicine Department of Sun Yat-Sen University (Guangzhou, China), and were free of mycoplasma contamination.
Plasmids and transfection
IGFBP7 expression plasmid was generated by PCR sub-cloning of human IGFBP7 coding sequence into retroviral transfer plasmid pMSCV to generate plasmid pMSCV-retro-puro-IGFBP7. For depletion of IGFBP7, two human shRNA sequences were cloned into the pSuper-retro-puro plasmid to generate pSuper-retro-IGFBP7-RNAi(s), respectively. Retroviral production and infection were performed as previously described , and stable cell lines were selected by treatment with 0.5 μg/ml puromycin for 10–14 days, beginning at 48 h after infection.
Western blotting analysis
Western blotting analysis was performed according to a standard method previously described , using anti-IGFBP7, anti-p21, anti-p27, anti-CDK2, anti-Cyclin E, anti-phosphor-Rb (Ser780) and anti-Rb, anti-AKT, anti-phosphor-AKT (Ser473) and anti-phosphor-AKT (Thr308) antibodies. Blotted membranes were stripped and re-blotted with an anti-α-tubulin mouse monoclonal antibody (Sigma–Aldrich, St. Louis, MO) used as a loading control.
3-(4,5-Dimethyl-2-thiazolyl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) assay
According to previous studies , cell viability was determined using an MTT assay. The cells were seeded at a density of 5 × 103 cells per well in 96-well plates. Subsequently at 1, 2, 3, 4, 5 and 6 days, 20 μl MTT (Sigma–Aldrich, St. Louis, MO) was added to each well and incubated for 4 h. The culture medium was removed, and 200 μl dimethyl sulfoxide (DMSO) (Amresco, Solon, Ohio) was added to each well. The plates were then shaken at room temperature for 10 min, and the absorbance of stained cells was measured at 570 nm, with 655 nm as the reference wavelength. Each experiment was performed in triplicates and repeated for three times.
Colony formation and soft agar assays
For the 2-D colony formation assay, cells were plated into 6-well plates at the density of 200–500 per well. The cells were allowed to grow for 7–12 days and stained with crystal violet. The plates were photographed and the numbers of colonies formed by indicated cells were quantified using the Quantity One software package (Bio-Rad, Hercules, CA). For the soft agar assays, one or three thousand cells were trypsinized and suspended in 2 ml of culture medium containing 0.3% agar (Sigma). The agar–cell mixture was grown on top of 1% agar contained in culture medium. After 10 days, viable cellular colonies larger than the indicated diameter were counted. Each experiment was repeated for three times.
Bromodeoxyuridine labeling and immunofluorescence
Cells were plated on coverslips (Fisher, Pittsburgh, PA). After 24 h, cells were incubated with bromodeoxyuridine (BrdU) for 1 h and stained with anti-BrdU antibody (Upstate, Temecula, CA) according to the manufacturer’s instruction. Immunostaining images were acquired under a laser scanning microscope (Axioskop 2 plus, Carl Zeiss Co. Ltd., Jena, Germany). Each experiment was repeated for three times.
Cells were harvested, washed with cold PBS and processed for cell cycle analysis using flow cytometry. Briefly, the cells were fixed in 75% ethanol and stored at − 20 °C for later analysis. The fixed cells were centrifuged at 1000 rpm and washed with cold PBS twice. RNase A (20 μg/ml final concentration) and propidium iodide staining solution (50 μg/ml final concentration) was added to the cells and incubated for 30 min at 37 °C in the dark. Fifty thousand cells were analyzed using a FACSC alibur instrument (BD Biosciences, San Jose, CA) equipped with CellQuest 3.3 software. ModFit LT 3.1 trial cell cycle analysis software was used to determine the percentage of cells in the different phases of the cell cycle. Each experiment was repeated for three times.
Immunohistochemical analysis (IHC)
A total of 112 paraffin-embedded thyroid tumor samples described above were used in the current study. For the use of these clinical materials for research purposes, prior patients’ consents and approval from the Institutional Research Ethics Committee were obtained. After deparaffinization, sections were immunostained using anti-IGFBP7 monoclonal antibody. The resultant immunostaining images were captured using the AxioVision Rel.4.6 computerized image analysis system (Carl Zeiss, Oberkochen, Germany). The procedure was carried out according to previously described methods . The degree of immunostaining of formalin-fixed, paraffin-embedded sections was reviewed and scored independently by two investigators, based on both the proportion of positively-stained tumor cells and the intensity of staining. The observers were blinded to the histopathological features and patient data of the samples.
AKT kinase activity detection
The AKT Kinase Assay kit was purchased from the Cell Signaling (Danvers, MA, # 9840). As instructed by the provided protocol, immobilized AKT antibody was used to immune-precipitate AKT from the indicated cell extracts . Immune-precipitated pellets were then incubated in the Kinase Buffer containing GSK-3 fusion protein and cold ATP. Levels of GSK-3 phosphorylation using the anti-phospho-GSK-3α/β (Ser21/9) antibody were measured by western blotting and chemiluminescent detection. All the experimental steps were carried out strictly according to the instructions of the kit. Each experiment was repeated for three times.
In vivo tumor growth assay
For the in vivo tumor growth assay, ARO-Vector and ARO-IGFBP7cells (2x106 cells each), FRO-Vector and FRO-IGFBP7 cells (5 × 106 cells each), WRO-Vector and WRO-IGFBP7 (8 × 107 cells each), WRO-RNAi-Vector and WRO-IGFBP7-RNAi-2 (7 × 107 cells each) were subcutaneously inoculated into the dorsal thighs of individual female BALB/C nude mice (6–7 weeks of age, 20–24 g). Tumor lengths (L) and widths (W) were measured every 2 days using a digital caliper, and tumor volumes were calculated using the equation volume (mm3) = L*W2/2. After 3–4 weeks, mice were anesthetized and sacrificed, and tumors were removed completely, photographed and weighed. The tumor growth curves were plotted and statistically analyzed. The measurement data were expressed as mean value plus standard deviation (X ± S). The comparison between the two groups was conducted by t test. Moreover, the tumors were sectioned for HE staining and immunostaining of Ki-67. Animal experiments were approved by the Ethical Committee of Sun Yat-sen University.
All statistical analyses were performed with the SPSS 20.0 software package (IBM, Chicago, IL, USA). Comparative analysis between groups was performed with two-tailed paired Student’s t test for statistical significance. The Chi square test was used to analyze the relationship between IGFBP7 expression and pathological characteristics. All bars represent the mean ± SD derived from three independent experiments. P values < 0.05 were considered significant.
This work was supported by the National Key Research and Development Program of China (2017YFA0106300); the Natural Science Foundation of China (81870069, 81500279, 81772473, 81472351); the Natural Science Foundation of Guangdong Province (2016A030306026); Pearl River S&T Nova Program of Guangzhou (201610010177).
LZ, YH and JC conceived and designed study. RL, JZ, XF, RY and LP collected the related paper. LZ, RL and YH designed and executed the experiments. ML, JW and JC participated in the design of the manuscript. LZ and RL wrote the manuscript. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
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