Background
Lung cancer ranks first among all malignant tumors in terms of morbidity and mortality, posing a major threat to human health [
1,
2]. Lung adenocarcinoma (LUAD) is one of the most common subtypes of lung cancer, accounting for 30–35% of primary lung cancers [
3]. Although tremendous efforts have been devoted to fighting against lung cancer, limited improvement in survival has been achieved. Recently, molecular targeted therapy has shown promising results in treating LUAD [
4‐
6], prompting researchers to explore new molecular mechanisms in LUAD.
Aerobic glycolysis, also known as Warburg effect, refers to the conversion of glucose into lactate in cancer cells even under sufficient oxygen conditions [
7]. Accumulating evidence has demonstrated that glycolysis contributes to tumor growth and metastasis through such unique metabolic pathway. Herein, it is a new strategy to delay tumor progression by inhibiting glycolysis in cancer cells [
8].
Hexokinases (HKs) are a family of enzymes that catalyze the first step in glucose metabolism by phosphorylating glucose to glucose-6-phosphatase of glucose utilization [
9]. So far, four HK isozymes have been identified in mammals, named from HK I to HK IV. Among the four isoforms of HKs, HK2 is the most widely studied and a key player in aerobic glycolysis in cancers. Overexpression of HK2 is also observed in liver cancer [
10], colorectal cancer [
11], prostate cancer [
12], and esophageal squamous cell carcinoma [
13], and is associated with poor prognosis in patients. Moreover, HK2 is also reported to be upregulated and to function as a novel oncogene in lung cancer [
14,
15].
Hexokinase domain component 1 (HKDC1) is a recently discovered protein, that is categorized as a putative fifth hexokinase [
16]. Under physiological conditions, HKDC1 is extremely critical to maintain whole-body glucose homeostasis [
17‐
19]. However, aberrant expression of HKDC1 contributes to the progression of certain types of diseases and cancers. For example, overexpression of HKDC1 could lead to the metabolic dysfunction of hepatocytes, which may be associated with nonalcoholic fatty liver disease [
20]. In addition, increasing evidence shows that HKDC1 may play oncogenic roles in cancers, such as lymphoma [
21], liver cancer [
22], breast cancer [
23] and colorectal cancer [
24], indicating that HKDC1 may serve as a therapeutic target in cancers.
Previous bioinformatics analysis predicted that HKDC1 could be a promising therapeutic target for lung cancer [
25]. However, this hypothesis remains to be validated, and the downstream mechanism of HKDC1 in lung cancer needs to be explored. In this study, we performed a series of functional assays in vitro and in vivo to investigate the roles of HKDC1 in LUAD.
Methods
Cell culture
The LUAD cell lines A549 and H1299, and the normal human bronchial epithelial cell line HBE were obtained from the Chinese Academy of Sciences Cell Bank (Shanghai, China) and cultured in Dulbecco’s modified Eagle medium (DMEM) (Invitrogen, Carlsbad, CA) containing 10% fetal bovine serum (FBS) (Invitrogen) at 37 °C in a humidified atmosphere of 5% CO2.
Clinical tissue and specimens
A total of 20 fresh primary LUAD tissues and paired adjacent normal tissues were obtained from surgeries at Changhai Hospital, Second Military Medical University (Shanghai, China). Seventy-five paired paraffin-embedded LUAD specimens used in this study were collected from patients in 2013 who were diagnosed with primary LUAD and none of them received preoperative chemotherapy or radiotherapy. Overall survival (OS) was defined as the interval between surgery and death or last observation. This study was approved by the Ethics Committee of Changhai Hospital. All patients provided written informed consent upon enrolment.
Construction of reagents for gene overexpression and knockdown
We constructed lentiviral vectors encoding the human HKDC1 gene or green fluorescent protein (GFP) in the pLenti-EF1a-EGFP-P2A-Puro-CMV-MCS-3Flag vector (HeYuan Bio-technology Co., Shanghai, China), which were named ov-HKDC1 or ov-NC. Stable LUAD cell knockdown of HKDC1 was generated using lentiviral constructs expressing sh-HKDC1 (sh-HKDC1#1: GGTGGACAGGTTCCTGTAT), sh-HKDC1#2: GGTCAGTGCGAATGTACAA) or sh-NC. LUAD cells were infected for 48 h and then selected with puromycin. Stable LUAD cell lines were successfully established if the infection efficiency was > 85%.
Immunohistochemistry (IHC)
The LUAD tissue slides were incubated with anti-HKDC1 (1:200, Abcam, ab228729) primary antibody. IHC scoring was performed using a modified Histo-score (H-score) by two independent pathologists. Briefly, the proportion of positively stained cells was scored as 0–100% (< 25% scored 0, 25–50% scored 1, 50–75% scored 2, 75–100% scored 3) and the intensity score was scored as 0 (negative), 1+ (weakly positive), 2+ (moderately positive), or 3+ (strongly positive). A final score was then calculated by multiplying these two scores.
RNA extraction and quantitative RT-PCR (qRT-PCR)
Total RNA was extracted from cultured LUAD cell lines or tissue specimens using TRIzol (Invitrogen, Grand Island, NY) according to the manufacturer’s instructions. The cDNA was synthesized using the PrimeScript RT Reagent Kit (TaKaRa Bio, Shiga, Japan) following the manufacturer’s instructions. Real-time PCR was performed on a Roche Light Cycler 480 (Roche) using SYBR Green PCR Master Mix (TaKaRa Bio, Shiga, Japan). The fold change relative to the mean value was determined by 2−ΔΔCt. All experiments were performed in triplicate. Primer sequences are listed as follows.
HKDC1:
5′-ATCCTGGCAAGCAGAGATACG-3′ (forward).
5′-GACGCTCTGAAATCTGCCCT-3′ (reverse);
GAPDH:
5′-GGAGCGAGATCCCTCCAAAAT-3′ (forward).
5′-GGCTGTTGTCATACTTCTCATGG-3′ (reverse);
Western blotting
Whole cultured cells were homogenized in 0.1% SDS and 1 mM PMSF. Protein extracts were subjected to SDS-PAGE and analyzed using the following primary antibodies against the following antigens: HKDC1 (Abcam, ab228729), phospho-AMPKα (Cell Signaling Technology, 2535), phospho-mTOR (Cell Signaling Technology, 5536), phospho-p70S6 (Cell Signaling Technology, 9234), Vimentin (Santa Cruz, sc-6260), Snail (CST, 3879), E-cadherin (Abcam, ab40772), N-cadherin (Abcam, ab18203) and GAPDH (Abcam, ab8245). Then, the membranes were incubated with secondary antibodies (CST, 7076, 7074) at room temperature for 1 h. All experiments were performed in triplicate. The results of western blotting bands were quantified by measuring the gray values (ImageJ software, Rawak Software Inc, Stuttgart, Germany).
Reagents
AICAR (CST, 9944) was used to activate AMPK signaling and rapamycin (Abcam, ab120224) was used to inhibit mTOR signaling in LUAD cells. LUAD cells were incubated at 37 °C for 24 h with 3 mM AICAR and 100 μM rapamycin for subsequent experiments.
Measurement of glucose and lactate
Transfected A549 and H1299 cells were seeded in 6-well plates (5 × 105) and the culture media were harvested 48 h after transfection. The glucose and lactate levels were measured using a Glucose Assay Kit (Sigma-Aldrich, USA) and a Lactic Acid Assay Kit (Sigma-Aldrich, USA), respectively, according to the manufacturer’s protocol. The values were normalized to the total protein concentration. All experiments were performed in triplicate.
Cell proliferation assays
Cell viability was measured by Cell Counting Kit-8 (CCK-8, Bimake, USA). Briefly, transfected cells were seeded in 96-well plates (5000 cells/well) and cultured for 3 days to assess proliferation. The absorbance was measured at 450 nm. All experiments were performed in triplicate.
Cell migration and invasion assay
Cell migration and invasion ability was assessed by 24-well Transwell chambers (Corning) with or without a Matrigel (Corning, Bedford, MA, USA) coating. Briefly, approximately 1 * 105 cells were resuspended in 300 µL serum-free DMEM and seeded into the upper chambers, whereas the bottom chamber was filled with 500 µL 10% FBS medium. Twenty-four hours later, the migrated/invaded cells in the lower chamber were fixed with 4% paraformaldehyde and stained with 1% crystal violet. All experiments were performed in triplicate. Cell counting was accomplished by ImageJ software (Rawak Software Inc, Stuttgart, Germany).
Xenograft mice
Five-week-old male BALB/c nude mice were purchased from Shanghai Experimental Center (Shanghai, China). Xenograft tumor models were established by subcutaneous injection of ovHKDC1 or shHKDC1 (5 × 106) transfected A549 cells into the right dorsal flank. Three mice were randomly assigned to each group. One week after injection, the mice were measured once a week for a total of 4–5 weeks. Tumor volume (V, cm3) was evaluated by a slide caliper (Shanghai, China) based on tumor length (L) and width (W) with the following formula: V = 1/2 × L × W2. All manipulations were performed in accordance with currently prescribed guidelines and under a protocol approved by the SMMU Ethical Review Committee (Shanghai, China).
Statistical analysis
Data analysis was carried out using IBM SSPS 24 (IBM Corp., Armonk, NY, USA) and data were reported as the mean ± standard deviation (mean ± SD). Student’s t-test was used to determine differences between groups and two-tailed ANOVA was performed in cases of multiple groups. The association between genes and clinicopathological features was analyzed by the Chi-square test or Fisher’s exact test. Kaplan–Meier curves were used to compare the OS between groups. Multivariate analysis was performed to determine independent factors affecting the prognosis of patients. Differences were considered statistically significant when p < 0.05.
Discussion
In this study, we discovered that HKDC1 was highly expressed in LUAD tissues and cell lines, and the positive expression of HKDC1 was correlated with aberrant clinicopathological characteristics in LUAD patients. In addition, HKDC1 could serve as an OS predictor for LUAD patients. Overexpression of HKDC1 promoted the proliferation, migration, invasion, glycolysis, EMT and tumorgenicity in vitro and in vivo, whereas knockdown of HKDC1 produced the opposite functional effects. Mechanistically, HKDC1 could regulate AMPK/mTOR signaling pathway to perform its biological function. Targeting HKDC1 may provide a new therapeutic strategy for LUAD treatment.
Li and colleagues screened the top 20 genes with potential of being developed into candidate therapeutic targets of lung cancer, among which 19 genes were targeted by approved drugs or drugs used in clinical trials [
25]. HKDC1 was the only one that was not included in these 20 candidate targets, which attracted our interest. Moreover, the role of HKDC1 as an oncogene in liver cancer and colorectal cancer prompted us to investigate its functional effect in LUAD. In the present study, we found that HKDC1 was highly expressed in LUAD tissues while was not expressed or lowly expressed in adjacent normal lung epithelial tissues, and its expression was correlated with aberrant clinicopathological characteristics and prognosis. These data preliminarily revealed that HKDC1 had an oncogenic function in LUAD and these unique properties make it a perfect therapeutic target for LUAD.
Metabolic reprogramming, such as glycolysis under aerobic conditions, has been increasingly deemed a hallmark for tumor progression in multiple cancers [
30]. Elevated glycolysis in cancer cells promotes glucose uptake and lactate production to fulfil their metabolic demands, followed by the increased invasion and metastasis abilities. It has been reported recently that HKDC1 catalyzes glucose phosphorylation and cellular energy metabolism involving cancer growth and metastasis [
23]. In our study, we observed that HKDC1 increased glucose consumption and lactate production, indicating HKDC1 could regulate aerobic glycolysis in LUAD. Chen et al. found that HKDC1 was located on the mitochondrial membrane and regulated the permeability transition pore opening, suggesting a reasonable mechanism for the metabolic effect of HKDC1 [
23].
Previous studies have demonstrated that HKDC1 is associated with aggressive phenotype and poor prognosis in HCC [
22]. Further, HKDC1 modulates the oxidative stress, apoptosis, proliferation, and metastasis in breast cancer [
23]. In our study, we also observed that HKDC1 promoted the proliferation, invasion and EMT capacity in vitro and tumor growth in vivo. These findings demonstrated that HKDC1 could function as an oncogene in LUAD, which provides more evidence that it may serve as a therapeutic target for LUAD.
HKDC1 affects behavioral functions in cancers by different mechanisms. For instance, Chen et al. discovered that HKDC1 knockdown significantly suppressed extranodal nasal-type natural killer/T-cell lymphoma growth through ROS generation and DNA damage [
21]. Zhang et al. found that silencing HKDC1 may inhibit cellular proliferation and migration by suppressing Wnt/β-catenin signaling pathway in HCC [
22]. In the present study, we determined the oncogenic functions of HKDC1 in LUAD. However, the downstream mechanisms by which HKDC1 influenced LUAD progression were still vague. Thus, we next explored its potential regulatory pathway in LUAD. AMPK is a sensor of energy status that maintains cellular energy homeostasis, which contributes to the regulation of mitochondrial biogenesis and disposal, cell polarity, cell growth and proliferation [
31]. mTOR, a central integrator of nutrient and growth factors, is negatively regulated by AMPK, which in turn promotes processes including the cell cycle, cell growth and angiogenesis [
32]. AMPK/mTOR signaling pathway is dysregulated in most human cancers and has been considered a promising therapeutic target against cancers [
33,
34]. Based on the observation that HKDC1 could promote the aerobic glycolysis in LUAD, we speculated that AMPK/mTOR pathway may mediate the oncogenic functions of HKDC1. To test the effect of HKDC1 on this pathway, western blotting was used to examine the expression of the key factors of the signaling pathway. As expected, HKDC1 overexpression resulted in decreased p-AMPK expression, and increased p-mTOR and p-70S6 expression. More importantly, activating AMPK by AICAR or blocking mTORC1 by rapamycin attenuated the biological effect of HKDC1 on LUAD cells, indicating biological role of HKDC1 was mediated by AMPK/ mTOR signal pathway.
In conclusion, our study demonstrates that HKDC1 plays an oncogenic role in LUAD. Targeting this gene may provide a promising therapeutic target to delay LUAD progression.
Conclusions
HKDC1 is highly expressed in lung adenocarcinoma (LUAD) and could serve as a prognostic predictor for LUAD patients. Overexpression of HKDC1 promotes the proliferation, migration, invasion, glycolysis, EMT and tumorgenicity of LUAD via activating AMPK/mTOR signaling pathway. Thus, HKDC1 may be a promising therapeutic target of LUAD.
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