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Oncotarget. 2017 February 28; 8(9): 14537–14548.
Published online 2017 January 14. doi:  10.18632/oncotarget.14653
PMCID: PMC5362424

Transcription factor HBP1 is a direct anti-cancer target of transcription factor FOXO1 in invasive oral cancer


Either FOXO1 or HBP1 transcription factor is a downstream effector of the PI3K/Akt pathway and associated with tumorigenesis. However, the relationship between FOXO1 and HBP1 in oral cancer remains unclear. Analysis of 30 oral tumor specimens revealed that mean mRNA levels of both FOXO1 and HBP1 in non-invasive and invasive oral tumors were found to be significantly lower than that of the control tissues, and the status of low FOXO1 and HBP1 (< 0.3 fold of the control) was associated with invasiveness of oral tumors. To investigate if HBP1 is a direct transcription target of FOXO1, we searched potential FOXO1 binding sites in the HBP1 promoter using the MAPPER Search Engine, and two putative FOXO1 binding sites located in the HBP1 promoter –132 to –125 bp and –343 to –336 bp were predicted. These binding sites were then confirmed by both reporter gene assays and the in cellulo ChIP assay. In addition, Akt activity manipulated by PI3K inhibitor LY294002 or Akt mutants was shown to negatively affect FOXO1-mediated HBP1 promoter activation and gene expression. Last, the biological significance of the FOXO1-HBP1 axis in oral cancer malignancy was evaluated in cell growth, colony formation, and invasiveness. The results indicated that HBP1 knockdown potently promoted malignant phenotypes of oral cancer and the suppressive effect of FOXO1 on cell growth, colony formation, and invasion was alleviated upon HBP1 knockdown in invasive oral cancer cells. Taken together, our data provide evidence for HBP1 as a direct downstream target of FOXO1 in oral cancer malignancy.

Keywords: FOXO1, HBP1, oral cancer


The forkhead box O (FOXO) transcription factor family shares a conserved ‘forkhead box’ DNA-binding domain and is consisted of four members in mammals: FOXO1, FOXO3a, FOXO4 and FOXO6 [1]. FOXO factors are involved in a wide range of biological processes, including cell cycle arrest, apoptosis, DNA repair, glucose metabolism, oxidative stress resistance and longevity [1]. The biological activity of FOXO factors is mostly dependent on the post-translational modification of phosphorylation, acetylation, or ubiquitination, thereby determining their intracellular trafficking [2]. Among FOXO factors, increased p-FOXO1 or decreased FOXO1 expression is often associated with tumorigenesis [3]. FOXO1 may exert its tumor suppression function through its transcription-dependent expression of growth arrest and apoptotic-related genes, including p15, p19, NOXA, FasL, TRAIL, and Bim [46]. The promoters of these genes comprise the FOXO-recognized element with the consensus sequence T/C-G/A-A-A-A-C-A-A [7]. Together, FOXO1 appears to be a potential therapeutic target of anticancer reagents.

HMG box-containing protein 1 (HBP1) is a regulator of cell cycle exit and cell differentiation [8]. Overexpression of HBP1 leads to an inhibition of the G1-S phase transition [9]. Loss-of-function HBP1 variants have been isolated in myeloid leukemia and breast cancers [10, 11]. Conversely, ectopic or chemical-induced expression of HBP1 results in growth arrest, apoptosis, or differentiation in cancer cell lines, including oral cancer [1215]. Together, these findings suggest a role of HBP1 in tumor suppression. HBP1 exerts its repression function through an HMG box DNA-binding domain and an AXH transcriptional repression domain. Genes down-regulated by HBP1 include p47phox, N-myc, c-myc, CCND1, and MIF [9, 14, 16, 17].

Studies of HBP1 have been focused on the finding of its transcription downstream targets. How the HBP1 promoter is regulated remains unclear. In a previous study, we demonstrated that HBP1 is a downstream effector of the EGFR (epidermal growth factor receptor))/Akt pathway in oral cancer [15]. Subsequently, a recent report illustrated that HBP1 is direct target of growth factors-mediated PI3K/Akt/FOXO pathway in various types of cancer [18]; however, whether or not FOXO1 regulates HBP1 expression in oral cancer remains unclear. In this study, we reported that both HBP1 and FOXO1 were down-regulated in a subset of oral tumor specimen. Ectopic expression of FOXO1 led to increased HBP1 promoter activity and HBP1 expression in oral cancer cells. Indeed, FOXO1-influencing factors, such as Akt activity, also accordingly affect HBP1 promoter activity and HBP1 expression. The direct binding of FOXO1 onto the HBP1 promoter was evidenced by the identification of two putative FOXO1 consensus sites in its cis-acting region. Furthermore, the biological significance of FOXO1-mediated HBP1 expression was demonstrated by the experiments of colony formation and cell invasion in oral cancer cells. Together, the current study provided evidence that FOXO1 and HBP1 function coordinately as tumor suppressors in invasive oral cancer.


Low FOXO1/low HBP1 expression predicts invasiveness of oral cancer

FOXOs transcription activity is tightly regulated by the Akt signaling [19]. Previously, we demonstrated that HBP1 functions as a downstream effector of the EGFR/Akt signaling pathway in oral cancer [15]. Both FOXOs and HBP1 are negatively regulated by Akt. FOXOs are directly modified by Akt phosphorylation for subsequent degradation; however, how HBP1 expression is down-regulated by Akt remains unclear in oral cancer. Using the MAPPER Search Engine to predict the putative transcription factor binding sites (TFBSs) in the HBP1 promoter, we identified several potential FOXO1 binding sites in the proximal region of the HBP1 promoter. Therefore, we hypothesized that FOXOs may play a crucial role in Akt-mediated suppression of HBP1 expression. Hence, the current study is aimed at investigating the putative transcriptional regulation of HBP1 by FOXO1 and, collectively, the biological significance of FOXO1 and HBP1 in oral cancer.

First, we examined the association of FOXO1 and HBP1 with oral tumorigenicity by comparing the mRNA levels of FOXO1 and HBP1 from 30 oral tumor specimens obtained from China Medical University Hospital (Taichung, Taiwan) with those of nine normal tissues. The mean mRNA level of either HBP1 or FOXO1 in non-invasive and invasive oral tumors (lymph node metastasis) was significantly lower than those of control normal tissues (Figure (Figure1A).1A). Reduced expression of both FOXO1 and HBP1 was also found in two tongue squamous cell carcinoma datasets in the Oncomine database (Supplementary Figure 1). Further analysis indicated a correlation of a low-HBP1 and FOXO1 status (< 0.3 fold) with the aggressiveness of oral tumors (Figure (Figure1B).1B). Indeed, when we tested the correlation between HBP1 and FOXO1 expression in aggressive oral cancer specimens, we found that HBP1 mRNA levels were positively correlated with FOXO1 mRNA levels in invasive oral cancer (Figure (Figure1C).1C). Furthermore, both FOXO1 and HBP1 mRNA levels were significantly lower in three EGFR over-expressing oral cancer cells tested than the normal human oral keratinocyte (HOK) (Figure (Figure1D).1D). These clinical data suggest that a combination of low HBP1 and low FOXO1 status might determine oral cancer malignancy, and that HBP1 and FOXO1 expression might be coordinately regulated.

Figure 1
Coordinate down-regulation of FOXO1 and HBP1 in oral cancer

FOXO1 transcriptionally induces HBP1 expression

To illustrate FOXO1 regulation of HBP1 expression in oral cancer, first, we examined if HBP1 expression levels are in concert with FOXO1 levels. Ectopic expression of FOXO1 in HSC-3 cells with low endogenous FOXO1 levels (Figure (Figure2A)2A) resulted in increased expression of HBP1 protein and mRNA (Figure (Figure2B).2B). Similarly, knockdown of FOXO1 expression with FOXO1-specific siRNA led to reduced HBP1 expression in TW206 oral cancer cells with high level of endogenous FOXO1 (Figure (Figure2C).2C). These data suggest that HBP1 might be transcriptionally regulated by FOXO1. Indeed, ectopic expression of FOXO1 cDNA (0.2 and 0.4 μg) in 293T cells for 24 h enhanced the transcriptional activity of a 2-kb HBP1 promoter by 5 and 7 folds, respectively (Figure (Figure2D).2D). In addition, FOXO1 exhibited stronger activation of the 2-kb HBP1 promoter than FOXO3a (Figure (Figure2E)2E) although FOXO1 and FOXO3a share highly similar sequence [20]. FOXO1-induced activation of the 2-kb HBP1 promoter was also observed in HSC-3 oral cancer cells, and the induction was abolished when co-transfected with FOXO1-specific siRNA (Figure (Figure2F).2F). Taken together, these results indicate that FOXO1 is able to induce HBP1 expression through transcription.

Figure 2
FOXO1 induces HBP1 gene expression in oral cancer

FOXO1 activity is essential for the FOXO1-mediated HBP1 expression

The EGFR/PI3K/Akt signaling is often up-regulated in malignant oral cancer [21, 22]. Transcriptional activity of FOXO1 can be suppressed through Akt-mediated post-translational modifications [19]. In previous studies, we demonstrated that activation of Akt leads to down-regulation of HBP1 expression (Figure (Figure4A4A in [15]), and inhibition of Akt phosphorylation by LY294002, a chemical inhibitor of PI3K, results in increased protein level of FOXO1 (Figure (Figure4F4F in [23]). Hence, we studied whether FOXO1 activation of the HBP1 promoter is also under the control of the upstream regulator Akt in the HSC-3 oral cancer cell line with an aberrant activation of the EGFR/PI3K pathway [23]. Indeed, administration of LY294002 (20 μM) to HSC-3 cells potently suppressed Akt and FOXO1 phosphorylation with a concomitant increase in HBP1 protein expression (Figure (Figure3A).3A). LY294002 also caused increased mRNA level of HBP1 in HSC-3 cells (Figure (Figure3B).3B). In addition, the reporter gene assay revealed that LY294002 enhanced the FOXO1-mediated HBP1 promoter activity in a dose-dependent fashion (Figure (Figure3C).3C). Then we tested the direct effect of Akt on FOXO1-mediated HBP1 expression. Overexpression of either wild-type (Akt1) or constitutively active Akt1 (Myr-Akt1) potently abolished FOXO1-induced activation of the 2-kb HBP1 promoter (upper panel, Figure Figure3D)3D) and the expression of HBP1 protein (lower panel, Figure Figure3D).3D). However, the Akt mutant (Akt1 T308A/S473A) had no significant effect on FOXO1-mediated activation of HBP1 promoter and protein expression (Figure (Figure3D).3D). These results suggest that Akt phosphorylation of FOXO1 might modulate the transcriptional activity of the HBP1 promoter. We further employed FOXO1-AAA, a constitutively active FOXO1 mutant, with triple mutation on the Akt phosphorylation sites, T24A, S256A, and S319A, [24] to test this hypothesis. FOXO1-AAA overexpression showed a stronger enhancement effect on the promoter activity of HBP1 than that of wild-type FOXO1 overexpression in HEK 293T cells (Figure (Figure3E).3E). In addition, the result from the DNA-binding defective FOXO1 (H215R) [24] indicated that this domain is also crucial for the full activation of FOXO1 on the HBP1 promoter (Figure (Figure3E).3E). These data demonstrated that both the protein activity and its DNA-binding ability of FOXO1 are crucial for the FOXO1-mediated HBP1 activation. In addition, the FOXO1-HBP1 axis is a crucial downstream effector of the EGFR/PI3K/Akt signaling pathway in oral cancer.

Figure 3
HBP1 expression is regulated by FOXO1 activity
Figure 4
Identification of FOXO1 response elements in the HBP1 promoter

Identification of the FOXO1 response elements in the HBP1 promoter

Next, we studied if the regulation of FOXO1 in the transcription of HBP1 is through direct binding to the HBP1 promoter. Three putative FOXO1 binding sites with a core recognition sequence (T/C/G)(G/A/T)AAA(C/A)A or TT(G/A)TTT(G/A)(G/C)[24, 25] were found on the upstream region –132 to –125, –343 to –336, and –380 to –373 bp from the HBP1 transcription start site (denoted as F1, F2, and F3, respectively) (Figure (Figure4A).4A). To test the effect of these potential FOXO1 binding sites, first, we co-transfected a pGL3-based luciferase reporter gene carrying a 0.2 kb, 0.5 kb, or 2 kb HBP1 promoter region along with various FOXO1 cDNA clones into HEK-293T cells, and we found that FOXO1 was able to enhance the HBP1 promoter activity of all three regions with a maximal activation for the 0.5 kb promoter (Figure (Figure4B).4B). This result suggests that FOXO1 binding sites might be located within the proximal region of the HBP1 promoter. To further differentiate and pinpoint the significance of these three potential FOXO1 sites, we carried out a serial deletion on F1, F2, and/or F3 in the 0.5 kb HBP1-luciferase reporter plasmid as depicted in Figure Figure4C.4C. Loss of F1, F2, or F3 diminished FOXO1-mediated activation, and the deletion of both F1 and F2 completely abolished FOXO1 activation of the HBP1 promoter (Figure (Figure4C).4C). Next we examined if FOXO3a also mediated the activity of the HBP1 promoter through these binding sites. As shown in Figure Figure4D,4D, F2 box is crucial for FOXO3a-mediated activation of the HBP1 promoter while both F1 and F2 boxes are important for FOXO1.

Lastly, to investigate whether FOXO1 binds to the human HBP1 promoter with the context of native human chromatin, chromatin immunoprecipitation (ChIP) assays were performed in HEK-293 cells [24]. Figure Figure5A5A depicted the 151 bp and 223 bp primer sets spanning the F1 and F2 boxes in the human HBP1 promoter starting at –125 bp and –336 bp, respectively, for the PCR analysis. FOXO1-Flag overexpression protein formed a complex with either region of the endogenous human HBP1 promoter, whereas the HBP1 promoter binding signal was barely detected in the negative control, GAPDH immunoprecipitation (Figure (Figure5B).5B). In contrast, FOXO1-ΔDB –Flag, lacking the DNA binding domain, obviously diminished the binding of FOXO1 to the human HBP1 promoter in HSC-3 cells (Figure (Figure5C).5C). These data confirm that FOXO1 binds to the native human HBP1 promoter in cellulo.

Figure 5
FOXO1 occupies its consensus binding sites in the endogenous HBP1 promoter

FOXO1-mediated activation of HBP1 expression suppresses tumor cell proliferation and invasion

Next, we examined whether FOXO1-mediated expression of HBP1 modulates tumorigenic growth and metastatic potential in oral cancer. As a downstream effector, HBP1 knockdown potently promoted cell malignancy as demonstrated by increased colony and invading cell numbers in HSC-3 cells (Figure (Figure6A).6A). Ectopic overexpression of constitutively active FOXO1 (FOXO1-AAA) significantly suppressed colony growth in HSC-3 oral cancer cells; however, HBP1 knockdown alleviated the suppressive effect of FOXO1-AAA on colony formation (Figure (Figure6B).6B). To further examine the role of FOXO1-mediated HBP1 expression in metastatic potential, both colony growth in soft agar and Matrigel invasion assay were performed in HSC-3 cells. Overexpression of either FOXO1 or HBP1 significantly decreased the ability of HSC-3 cells to form colonies in soft agar as compared with the vector control, while HBP1-specific siRNA diminished the suppressive effect of FOXO1 (Figure (Figure6C).6C). The data from the Matrigel invasion assay also exhibited the similar pattern (Figure (Figure6D).6D). Taken together, these data support HBP1 as a downstream target of FOXO1, which contributes to FOXO1-mediated inhibition of malignancy in oral cancer.

Figure 6
The role of FOXO1-mediated HBP1 expression in oral cancer malignancy


The PI3K/Akt pathway is commonly altered in human cancer [26]. The constitutive activation of the PI3K/Akt axis is mainly due to either gain-of-function mutations in PI3KCA, loss-of-function mutations in PTEN, or amplification of EGFR. Therefore, a large group of tumors with molecular alterations in the PI3K/Akt pathway is therapeutically targetable with PI3K inhibitors [27]. Growing evidence supports HBP1 as a key negative downstream regulator of the PI3K/Akt pathway. In a previous study, we demonstrated that HBP1 protein expression was down-regulated upon ectopic expression of a constitutive form of Akt in oral cancer cells [15]. In the present study, we further found that the PI3K inhibitor LY294002 significantly up-regulated HBP1 expression with a concomitant decrease in FOXO1 phosphorylation in HSC-3 oral cancer cells (Figure 3A–3B). Similar observation was also reported by Coomans de Brachene and colleagues that the PI3K inhibitor LY294002 or other Akt inhibitor (Akt inhibitor VIII or MK 2206) caused increased mRNA or protein expression of HBP1 in either eosinophilic leukemia or colon carcinoma cells [18]. In addition, HBP1 expression coincided with the FOXO activity under regulation by Akt inhibitor GSK690693 [28]. Concomitant reduction of mRNA expression levels of FOXO1 with HBP1 were also observed in a set of breast tumors [18]. In the current study, we found a decreased FOXO1 mRNA level in invasive oral tumor specimen, and the combination of decreased mRNA expression levels of FOXO1 and HBP1 may predict invasiveness of oral cancer.

Through direct binding to the consensus binding sites in the promoter regions, the FOXO transcription factors regulate the transcription of their target genes [29]. The potential FOXO1 binding sites in the HBP1 promoter were found –132 to –125, –343 to –336, and –380 to –373 bp upstream of the HBP1 transcription start site (denoted as F1, F2, and F3, respectively) (Figure (Figure4A)4A) using the MAPPER Search Engine ( Employing reporter genes carrying different regions of the HBP1 promoter, we found that a 0.5 kb HBP1 promoter, containing all three possible FOXO1 sites, displayed the strongest FOXO1 activation; however, a 0.2 kb promoter, which contains only one potential FOXO1 binding site, F1, was able to be stimulated by FOXO1, suggesting that this site is also a functional FOXO1 regulatory element (Figure (Figure4B).4B). Next we tested a series of single and combined deletions in the 0.5 kb HBP1 promoter, and our results indicated that F1 and F2 are the major FOXO1 sites, while F3 is necessary for the full FOXO1 activation of the HBP1 promoter (Figure (Figure4C).4C). Interestingly, FOXO1-H215R, a FOXO1 mutant defect in the DNA binding domain, was able to activate the HBP1 promoter although the induction was much weaker than that of the wild-type FOXO1 (Figure (Figure4B),4B), suggesting that HBP1 transcription can be regulated by FOXO1 through either direct or indirect binding. Indeed, FOXO1 can interact with other transcription factors to transcriptionally repress cyclin D1 (CCND1) and D2 (CCND2) [30] or activate cyclin G2 (CCNG2) and p130 (Rbl2) [31].

The HBP1 promoter seems to respond preferentially to FOXO1 than FOXO3a. To differentiate the role of FOXO1 and FOXO3a in the activation of the HBP1 promoter, a series of reporter gene assays were employed. The results revealed that FOXO1 is a stronger activator than FOXO3a for either 2-kb or 0.5-kb HBP1 promoter (Figures (Figures2E,2E, ,4D).4D). Of special note, although both FOXO1 and FOXO3a are able to induce the HBP1 promote activity, our data further indicate that the consensus binding site F2 is absolutely a prerequisite for the FOXO3a action on the HBP1 promoter (Figure (Figure4D),4D), which is in an agreement with the finding by Coomans de Brachene et al. [18]. However, in the absence of F2, the binding site F1 still contributed to at least 2-fold of the FOXO1 activation on the HBP1 promoter (Figure 4B–4D). Taken together, our data support FOXO1 as a crucial upstream regulator of the HBP1 gene transcription. Future study may reveal if the FOXO1-HBP1 axis and the FOXO3a-HBP1 axis share function redundancy, or one may be more active than the other under certain biological context.

Both FOXO1 and HBP1 are potential tumor suppressor genes; decreased FOXO1 expression [3] or loss-of-function HBP1 mutation [10, 11] is often associated with tumorigenesis. FOXO1 and HBP1 may exert their tumor suppression function through the induction of growth arrest and apoptosis [46, 12, 14, 15, 23]. Here, we showed that HBP1 can function as a downstream effector of FOXO1-mediated growth inhibition in oral cancer; HBP1 knockdown alleviated the suppressive effect of FOXO1 on colony formation (Figure 6B–6C). In addition, accumulated evidence also supports a role of FOXO1 and HBP1 in metastatic potential of cancer cells. Negative regulation of FOXO1 in cellular migration or invasion has been reported in various types of cancer, including prostate [32], and breast cancer [33]. Similarly, HBP1 knockdown hastens cell migration and invasion in breast and prostate cancer cells [11, 14]. In the current study, we further provide evidence that the FOXO1-HBP1 axis may suppress the invasiveness of oral cancer cells (Figure (Figure6D).6D). Take together, the FOXO1-HBP1 axis appears to be a potential therapeutic target of anticancer reagents in oral cancer.


Reagents and antibodies

All chemicals were purchased from Sigma (St. Louis, MO) and antibodies were from Santa Cruz Biotechnology (Santa Cruz, CA), respectively, unless specified otherwise. Antibody for HBP1 was from Novus Biologicals (Littleton, CO), and α-tubulin was from Abcam (Cambridge, MA). PVDF membranes and ECL detection reagents for Western blotting analysis were purchased from Perkin Elmer Life Sciences, Inc. (Waltham, MA). Dual-light® system was from Applied Biosystems (Foster City, CA). PI3K inhibitor LY 294002 was purchased from Sigma (St. Louis, MO). Small interfering RNA (siRNA) molecules specific for HBP1 was purchased from Invitrogen (Carlsbad, CA).


Expressing plasmids, including pcDNA3-Flag-FKHR(FOXO1)-Delta DB, pcDNA3-flag FKHRL1 (FOXO3a), pcDNA3-Flag-HA, pcDNA3-Flag-HA-Akt1, pcDNA3-Myr-HA-Akt1, and pcDNA3-T7-Akt1-T308A-S473A [34] were purchased from Addgene (Cambridge, MA, USA). The HBP1 expressing plasmid pEF-BOS-HA-HBP1, and FOXO1 expressing plasmids pcDNA3-A3-FOXO1-Flag pcDNA3-WT-FOXO1-Flag and pcDNA3-H215R-FOXO1-Flag were kindly provided by Dr. Amy S. Yee and Dr. Brian Schaffhausen (Tufts University, USA), respectively.

Cell culture and treatment

For human oral squamous carcinoma cell lines, HSC-3 and TW206 were kind gifts of Dr. Hsin-Ling Yang and SAS and OECM-1 cells were kindly provided by Dr. Jang-Chang Lee at China Medical University (Taichung, Taiwan). HOK human oral keratinocytes and HEK (Homo sapiens embryonic kidney)-293T cells were obtained from Drs. Shieh Tzong-Ming and Tzong-Der Way at China Medical University, respectively (Taichung, Taiwan). HSC-3 and OECM-1 cells were maintained in Dulbecco's Modified Eagle Medium (DMEM)/F-12 and RPMI 1640 medium, and SAS, and 293T cells were maintained in DMEM, respectively, supplemented with 10% fetal bovine serum (FBS) and 1% antibiotic-antimycotic. Cells were cultured in a 37°C, 5% CO2 incubator. All cell culture reagents were from Invitrogen (Carlsbad, CA), unless indicated otherwise.

Colony formation assay

HSC-3 cells after transfection were cultured in growth media in 60 mm dishes for 7 days, and then washed with PBS, fixed with 10% formalin (Mallinckrodt Chemicals, St. Louis, MO) for 10 min, and stained with 0.05% crystal violet (Panreac Quimica S.A.U.) for 30 min. Dishes were scanned for colony counting and crystal violet stain was dissolved in 100% methanol for optical density measurement at 540 nm.

Reporter assay

The pGL3-luc plasmids containing 2037 (2 kb), or 526 (0.5 kb), or 166 (0.2 kb) bp HBP1 promoter and RSV-β-galactosidase plasmids were kindly provided by Dr. Amy S. Yee, Tufts University, USA. HEK-293T cells (3 × 104 cells) cultured in a 24-well plate were transfected with pDL3-HBP1-luc (0.4 μg) and RSV-β- galactosidase (0.1 μg) along with indicated vectors for 24 h and then cell lysates were collected in lysis solution (Applied Biosystems, Carlsbad, CA) according to the manufacturer's protocol. The Dual Light® System (Applied Biosystems) was used to quantify luciferase and β-galactosidase activities.

Tissue sample preparation

As previously described, [35] fresh oral tumor specimens were collected from oral cancer patients and stored in liquid nitrogen. Tumor tissues containing > 85% tumor cells based on the staining results were qualified for further RNA extractions. Acquisition of tissue specimens was approved by the institutional review board of the China Medical University Hospital. A total of 30 oral tumor specimens was obtained from the tissue bank at China Medical University Hospital (Taichung, Taiwan). Total RNA extracted from 9 normal oral epithelial counterparts was used as reference samples. All 30 tumor specimens were divided into two groups, non-invasive (n = 18, pN = 0, no metastasis) and invasive (n = 12, pN > 0, lymph node metastasis).

Reverse transcription-polymerase chain reaction, real-time PCR, and PCR

Total RNA was extracted using RNeasy® Mini kit (Qiagen) according to the manufacturer's instructions. RT-PCR was performed using SuperScript™ III One-Step RT-PCR System with Platinum® Taq DNA Polymerase Kit (Invitrogen). The following primers were used: human HBP1, 5′-ATCATCTCCTGTACACATCATAGC-3′(F) and 5′-CATAGAAAGGGTGGTCCAGCTTAC-3′(R); 18S, 5′-GTCTGTGATGCCCTTAGATG-3′(F) and 5′-AGCT TATGACCCGCACTTAC-3′(R). Primer sequences for real-time PCR analysis of oral tumor specimens were: HBP1, 5′-GAACCAATTCAGGCTCACA-3′(F) and 5′-TC AAGACTCAATGCTATCAGTATC-3′(R); FOXO1, 5′-AA GAGCGTGCCCTACTTCAA-3′(F) and 5′-CTGTTGTT GTCCATGGATGC-3′(R). Primer sequences for PCR analysis in ChIP assays were: HBP1-125, 5′-TCTTTCG CCCTCTTATTGA-3′ (F) and 5′-GAACTGCCATTCGG TTCTTC-3′ (R); HBP1-336, F 5′-TTGTCCCAGACAC CAAAACA -3′(F) and 5′-GGATTGGACTATTGCCG AGA-3′(R).

Matrigel invasion assay [36]

Matrigel inserts for a 24-well chamber were purchased from BD Biosciences (Bedford, MA) and operated according to the manufacturer's protocol. HSC-3 cell suspensions (3 × 104 cells) after transfection with indicated plasmids were seeded onto the upper chamber in a serum-free medium and 10% FBS-containing medium was added to the lower chamber to serve as a chemoattractant. After 24 h of incubation in a 37°C, 5% CO2 incubator, the non-invading cells from the upper chamber were removed using cotton swabs while the invading cells on the lower surface were fixed with 100% methanol, stained (Giesma in 20% ethanol), and counted. The invading cells were photographed and counted in five, randomly selected microscopic fields (200X magnification). Cell invasion was photographed under 400× magnification. Error bars in Figure Figure6C6C represent the variation of the cell numbers between the selected fields.

Colony formation in soft agar [14]

HSC-3 cells (5 × 103 cells) after transfection with indicated constructs were suspended in 0.35% agar (DNA grade agarose, BIOMAN Scientific Co., Ltd, Taiwan) in DMEM containing 10% FBS and plated in 35 mm Petri dishes with a 0.5% agar bottom layer. After 14 days of incubation at 37°C in a humidified incubator, the colonies > 200 μm in diameter were counted microscopically within the field of a X40 objective lens (Olympus 1 × 71). Each bar represents the mean number of colonies (×40 field) ± S.E.M. from three independent experiments.

Chromatin immunoprecipitation (ChIP) assays

Cells transfected with empty vector or vectors encoding FOXO1-Flag or FOXO1-Delta DB were subjected to chromatin immunoprecipitation experiments performed with the Chromatin Immunoprecipitation (ChIP) Assay Kit (Millipore), following the manufacturer's instructions. Anti-Flag and control anti-GAPDH antibody were purchased from Santa Cruz Biotechnology (Santa Cruz, CA) and DNA was extracted using DNA extraction kit (Favorgen biotech corp., Taiwan). PCR reactions were conducted using the Fermentas PCR kit (Thermo scientific, PA, USA), following the cycling conditions: 1 cycle (95°C 2 min), 30 cycles (95°C 30 s, 58°C 30 s, 72°C 1 min), and 1 cycle (72°C 5 min) with the indicated primers. Migration of PCR products was performed in 2% agarose gels.

Statistical analysis

Data expressed as mean ± SD or mean ± SEM were calculated from at least three independent experiments. Statistical significance was analyzed using Student's t test. Results were considered significantly different at p < 0.05.



The authors thank Dr. Amy S. Yee (Tufts University, USA) for the 2-kb and 0.5-kb HBP1 promoter-luciferase reporter gene and β-galactosidase construct. This work was supported by the grants, NSC 98-2320-B-039-021-MY3 from Ministry of Science and Technology, and CMU97-108 from China Medical University, Taiwan, R.O.C., to Chun-Yin Huang, and NSC102-2320-B-309-001-MY3 from Ministry of Science and Technology, Taiwan, R.O.C. to Ming-Fen Lee.



None declared.


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