1. Department of Internal Medicine, Chi Mei Medical Center, Chiali, Taiwan
2. Departments of Colorectal Surgery, Yuan's General Hospital, Kaohsiung, Taiwan.
3. Department of Health Business Administration, Meiho University, Pingtung, Taiwan
4. Division of General Surgery, Chi Mei Medical Center, Tainan, Taiwan
5. Department of Health and Nutrition, Chia Nan University of Pharmacy & Science, Tainan, Taiwan
6. Department of Internal Medicine, Chi Mei Medical Center, Tainan, Taiwan
7. Department of Leisure, Recreation, and Tourism Management, Southern Taiwan University of Science and Technology, Tainan, Taiwan
8. Department of Radiation Oncology, Chi-Mei Medical Center, Liouying, Tainan, Taiwan
9. Department of Pathology, Chi Mei Medical Center, Tainan, Taiwan
10. Department of Anesthesiology, Chi Mei Medical Center, Tainan, Taiwan
11. National Institute of Cancer Research, National Health Research Institutes, Tainan, Taiwan
12. Department of Biotechnology, Southern Taiwan University of Science and Technology, Tainan, Taiwan
13. Institute of Clinical Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan
Purpose: Nasopharyngeal carcinoma (NPC) is a common cancer in southern China and Southeast Asia, but risk stratification and treatment outcome in NPC patients remain suboptimal. Our study identified and validated metabolic drivers that are relevant to the pathogenesis of NPC using a published transcriptome. Phosphoserine aminotransferase 1 (PSAT1) is an enzyme that is involved in serine biosynthesis, and its overexpression is associated with colon cancer, non-small cell lung cancer and breast cancer. However, its expression has not been systemically evaluated in patients with NPC.
Materials and Methods: We evaluated two public transcriptomes of NPC tissues and benign nasopharyngeal mucosal epithelial tissues that deposited in the NIH Gene Expression Omnibus database under accession number GSE34574 and GSE12452. We also performed immunohistochemical staining and assessment of PSAT1 in a total of 124 NPC patients received radiotherapy and were regularly followed-up until death or loss. The endpoints analyzed were local recurrence-free survival (LRFS), distant metastasis-free survival (DMFS), disease-specific survival (DSS), and overall survival (OS).
Results: We retrospectively evaluated 124 patients with NPC and found that high PSAT1 expression was associated with poor prognosis of NPC and indicator of advanced tumor stage. High PSAT1 expression also correlated with an aggressive clinical course, with significantly shorter DSS (HR= 2.856, 95% CI 1.599 to 5.101), DMFS (HR= 3.305, 95% CI 1.720 to 6.347), LRFS (HR= 2.834, 95% CI 1.376 to 5.835), and OS HR= 2.935, 95% CI 1.646-5.234) in multivariate analyses.
Conclusions: Our study showed that PSAT1 is a potential prognostic biomarker and higher expression of PSAT1 is associated with a poor prognosis in NPC.
Keywords: PSAT1, Nasopharyngeal carcinoma, prognosis
Nasopharyngeal carcinoma (NPC) is a common malignancy that originates in the nasopharynx, and it exhibits a complex biology that is not fully understood. The incidence of NPC is rare in most populations, such as Europe and the United States, but it is a common cancer in southern China and Southeast Asia1 and other populations, including the Middle East/North Africa and the Arctic. Genetics interact with the environment and contribute to the development of NPC because of the racial and ethnic geographical distribution of NPC worldwide2.
A previous study used published data in endemic areas and demonstrated that concurrent chemoradiotherapy was an effective treatment for locally advanced NPC and improved overall survival3. A study also showed neoadjuvant chemotherapy and concurrent chemoradiotherapy can reduce distant failure as compared with concurrent chemoradiotherapy alone4. However, the percentage of patients with distant metastases is high in NPC, and patients with distant metastases exhibit poor prognosis5-10. Accordingly, NPC management should consider individual patient differences using recognized prognostic factors. It is important to identify biomarkers that are independently associated with rapidly progressive tumors to designate an appropriate treatment.
It is getting clear that cancer cells acquire alterations in the metabolism of carbohydrates, proteins, lipids and nucleic acids to meet the requirements for rapid proliferation11. Cancer cells need high amounts of nonessential and essential amino acids to fuel essential anabolic processes. Growing evidence suggests that amino acid metabolic pathways are also chemotherapeutic targets12. We used the published transcriptome of NPC to find genes involved in tumorigenesis13 and demonstrated that phosphoserine aminotransferase 1 (PSAT1) was a prominently upregulated gene in the regulation of amino acid metabolism.
PSAT1 was observed in the brains and livers of sheep14. PSAT1 is involved in the second step of serine biosynthesis, and it converts 3-phosphohydroxypyruvate to L-phosphoserine15. PSAT1 plays an important role in metabolic functions. PSAT1 deficiency leads to seizures and acquired microcephaly16, and overexpression of PSAT1 correlates with cancer development17. However, information on the functions of PSAT1 in the regulation of cell proliferation and tumorigenesis and the association between PSAT1 overexpression and clinical implications in patients with NPC are not clear. Our study evaluated the influence of PAST1 expression on the clinical outcome of NPC patients.
We evaluated one public transcriptome containing expression profiling data of (GSE34574) which contains expression profiling data deposited in the NIH Gene Expression Omnibus database. The raw CEL files of Affymetrix HUMAN Genome U133 Plus 2.0 microarray platform were imported into Nexus Expression 3 software (BioDiscovery) to analyze all probe sets without pre-selection or filtering. Supervised comparative analyses and functional profiling were performed to identify significant differentially expressed genes, and special attention was paid to pathways involved in amino acid biosynthesis in Gene Ontology (GO:0008652). Genes with P≦0.01 and a log2-transformed expression fold change >1 were selected for further analysis. To crossly validate the findings, we also analyze another transcriptome dataset (GSE12452) for the selection of candidate gene as already been described in our previous publication18.
The institutional review board approved the procurement of formalin-fixed NPC tissue for this study (IRB10501-006). In brief, a total of 124 formalin-fixed paraffin-embedded tissue samples from NPC patients were used for PSAT1 immunohistochemical evaluations. These patients were regularly followed up by physicians after biopsy in the Chi-Mei Medical Center. Patients who were initially diagnosed with NPC without distant metastasis underwent tissue biopsy between January 1998 and December 2002. Two pathologists (C.F. Li and T.J Chen) classified tumors by histological type based on WHO classifications19. Tumor stage was adjusted according to the American Joint Committee on Cancer Tumor-Nodes-Metastasis (TNM) classification of malignant tumors20.
Formalin-fixed, paraffin-embedded tissue samples were cut into 4-μm-thick sections. Paraffin-embedded tissues were deparaffinized using xylene, rehydrated in ethanol, and heated in a microwave using methods described in our previous study21. Tissue samples were washed in Tris-buffered saline for 15 min, and slides were incubated with a primary monoclonal antibody against PSAT1 (1:100; Abcam).
All 124 NPC patients received a complete course of 3-dimensional radiotherapy (3DRT) in a constant protocol and were regularly followed-up until death or loss. The mean follow-up duration was 3 years. Patients with stage II-IV disease received concurrent cisplatin-based chemotherapy in addition to radiotherapy.
The SPSS 14 software package was used to perform statistical data analyses. Chi-square or Fisher's exact test analyzed the relationship between PSAT1 immunohistochemical expression and various clinicopathological parameters. The endpoints analyzed were local recurrence-free survival (LRFS), distant metastasis-free survival (DMFS), disease-specific survival (DSS), and overall survival (OS) which were calculated from the starting date of radiotherapy to the date of an event. Patients lost to follow-up were censored on the latest follow-up date. Multivariate analysis was performed using the Cox proportional hazards model. We also performed Kaplan-Meier analysis to compare the survival curves in NPC patients with different groups. The log-rank test was used to investigate differences in survival times between two groups. A P-value <0.05 was considered statistically significant.
Table 1 provides a summary of 8 significant differentially expressed genes associated with amino acid biosynthesis in the transcriptome of nasopharyngeal carcinomas (GSE34574). Of these, ASNS, PSPH, and PSAT1 exhibited upregulated mRNA expression and PSAT1 demonstrated the most significant upregulation (Logs ratio=4.2088, P<0.0001, Fig. 1). Interestingly, we also confirmed PSAT1 as the most significantly upregulated gene in an independent GEO dataset (GSE12452) which discloses PSAT1 upregulaiton is most associated with the development of NPC (tumor versus non-tumor, log2 ratio=2.0392, P<0.0001) in those associated with amino acid biosynthesis. Accordingly, we further evaluated the clinicopathological significance of PSAT1 expression by immunohistochemistry.
Summary of differentially expressed genes associated with amino acid biosynthesis in the transcriptome of nasopharyngeal carcinomas (GSE34574)
|Probe||Comparison 1 Log ratio (NPC vs. Non-tumor tissue)||p-value||Gene Symbol||Gene Name||Biological Process||Molecular Function|
|223062_s_at||4.2088||<0.0001||PSAT1||phosphoserine aminotransferase 1||L-serine biosynthetic process, amino acid biosynthetic process, metabolic process, pyridoxine biosynthetic process||catalytic activity, phosphoserine transaminase activity, pyridoxal phosphate binding, transaminase activity, transferase activity|
|205047_s_at||3.4002||<0.0001||ASNS||asparagine synthetase||amino acid biosynthetic process, asparagine biosynthetic process, glutamine metabolic process, metabolic process||asparagine synthase (glutamine-hydrolyzing) activity, ligase activity|
|217956_s_at||2.3727||0.0031||ENOPH1||enolase-phosphatase 1||amino acid biosynthetic process, metabolic process, methionine biosynthetic process||catalytic activity, hydrolase activity, magnesium ion binding, metal ion binding, phosphoglycolate phosphatase activity|
|203774_at||2.0694||0.0004||MTR||5-methyltetrahydrofolate-homocysteine methyltransferase||amino acid biosynthetic process, central nervous system development, folic acid and derivative biosynthetic process, methionine biosynthetic process, nervous system development||cobalamin binding, cobalt ion binding, dihydropteroate synthase activity, homocysteine S-methyltransferase activity, metal ion binding, methionine synthase activity, methyltransferase activity, protein binding, transferase activity, zinc ion binding|
|205048_s_at||1.543||0.0047||PSPH||phosphoserine phosphatase||L-serine biosynthetic process, L-serine metabolic process, amino acid biosynthetic process, cell proliferation, metabolic process||catalytic activity, hydrolase activity, magnesium ion binding, phosphoric monoester hydrolase activity, phosphoserine phosphatase activity, protein binding|
|203576_at||-1.3603||0.0002||BCAT2||branched chain aminotransferase 2; mitochondrial||amino acid biosynthetic process, branched chain family amino acid biosynthetic process, branched chain family amino acid catabolic process, branched chain family amino acid metabolic process, metabolic process||branched-chain-amino-acid transaminase activity, catalytic activity, transaminase activity, transferase activity|
|204608_at||-1.3908||0.0008||ASL||argininosuccinate lyase||amino acid biosynthetic process, arginine biosynthetic process, arginine biosynthetic process via ornithine, arginine catabolic process, urea cycle||argininosuccinate lyase activity, catalytic activity, lyase activity|
|207076_s_at||-3.6325||0.0001||ASS1||argininosuccinate synthetase 1||amino acid biosynthetic process, arginine biosynthetic process, urea cycle||ATP binding, argininosuccinate synthase activity, ligase activity, nucleotide binding, protein binding|
Published transcriptomic datasets of NPC versus benign nasopharyngeal tissues samples were evaluated. PSAT1 was an upregulated gene in the regulation of amino acid biosynthesis in the clustering analysis. Nasopharyngeal carcinoma (blue lines) and benign tissue (red lines) specimens are indicated at the top of the heatmap, and expression levels of upregulated and downregulated genes are expressed as a series of brightness of red and green colors, respectively. Unaltered mRNA expression is coded black.
Table 2 shows the associations between PAST1 expression and important clinicopathological variables. The 124 cases of NPC consisted of 5 keratinizing squamous cell carcinomas, 54 non-keratinizing differentiated carcinomas, and 65 undifferentiated carcinomas. There were 95 males and 29 females, and 26 cases were older than 60 years of age. Thirty-eight cases were classified as stages I and II, and 85 cases were classified as stages III and IV. The mean follow-up period was 3 years, and the median duration to tumor-associated mortality was 2 years. The median durations to distal metastasis and local recurrence were 10 and 16 months, respectively.
Low PAST1 expression was significantly associated with T1-T2 classification (P=0.024) and stages I-II classification (P=0.019), but it was not related to histological grade. Of all important clinicopathological paraneters, T3-4 status, N2-3 status and AJCC III-IV stages, and high PAST1 expression were all significantly predictive of worse outcomes for the three survival endpoints analyzed in univariate analyses (Table 3, Fig. 3). AJCC III-IV stages remained prognostically independent for DSS (P=0.041, hazard ratio [HR]= 2.072), LRFS (P=0.028, HR= 2.935), and OS (P= 0.036, HR= 2.108) in multivariate comparisons, but it lost statistical significance for DMeFS (Table 4). Moreover, high PAST1 expression also predictive a more aggressive clinical course, with significantly shorter DSS (HR= 2.856, 95% CI 1.599 to 5.101), DMeFS (HR= 3.305, 95% CI 1.720 to 6.347), LRFS (HR= 2.834, 95% CI 1.376 to 5.835), and OS (HR= 2.935, 95% CI 1.646-5.234) in multivariate analyses.
Associations between PSAT1 expression with other important clinicopathological variables.
|Low Exp.||High Exp.|
|Age (years)||<60 years||47||51||0.378|
|Primary tumor (T)||T1-T2||46||34||0.024*|
|Nodal status (N)||N0-N1||31||25||0.279|
PSAT1 is an aminotransferase that plays an important role in linking catabolic pathways (glycolysis) and amino acid (serine) biosynthesis. PSAT1 is responsible for the second step in serine synthesis, and it converts 3-phosphohydroxypyruvate to phosphoserine. Serine is an important carbon source for purine nucleotides, phosphatidylcholine, phosphatidylserine, and other cellular metabolites. Cancer cells use glucose and glutamine to support energy and anabolic metabolism22,23, and PSAT1 is overexpressed in some cancer cells. Cancer cells use non-amino acid precursors to synthesize glycine and serine, which was first noted in lymphomas24.
A previous study demonstrated that serine biosynthesis played an important role in bone metastatic breast cancer. Three enzymes, PSAT1, phosphoserine phosphatase (PSPH) and phosphoglycerate dehydrogenase (PHGDH), were responsible for the phosphorylated pathway of L-serine biosynthesis25. Jason et al. found that much of the glycolytic carbon in melanoma was redirected to serine and glycine metabolism via PHGDH. PSAT1 expression was also observed in melanoma26. PSAT1 is weakly expressed in normal colon tissue but is overexpressed in colon cancer, and its expression is associated with disease progression27-28. Yoon et al. followed 78 patients with recurrent colon cancer during a median follow-up duration of 55.5 months and found that PHGDH, pyruvate dehydrogenase kinase 1, and PSAT expression was significantly higher in tumor cells than normal tissue. Univariate analysis for recurrence-free survival in colon tumor cells demonstrated that pyruvate dehydrogenase kinase 2 positivity was the only positive prognostic factor, but there was no significant difference in multivariate analysis29.
Univariate log-rank analyses.
|Parameters||Category||No. of case||DSS||DMeFS||LRFS||OS|
|No. of event||p-value||No. of event||p-value||No. of event||p-value||No. of event||P-value|
|Age (years)||<60 years||98||48||0.8600||42||0.3091||29||0.8206||49||0.8049|
|Primary tumor (T)||T1-T2||80||32||0.0289*||25||0.0085*||19||0.0180*||32||0.0204*|
|Nodal status (N)||N0-N1||56||18||0.0008*||17||0.0132*||12||0.0160*||19||0.0011*|
|PAST1 Exp.||Low Exp.||60||17||<0.0001*||13||<0.0001*||11||0.0002*||17||<0.0001*|
*, Statistically significant; DSS, disease-specific survival; DMeFS, distal metastasis-free Survival; LRFS, local recurrence-free survival; OS, overall survival.
Multivariate survival analyses
|H.R||95% CI||p-value||H.R||95% CI||p-value||H.R||95% CI||p-value||H.R||95% CI||p-value|
|PAST1 Exp.||Low Exp.||1||-||<0.001*||1||<0.001*||1||-||0.005*||1||-||<0.001|
*, Statistically significant; DSS, disease-specific survival; DMeFS, distal metastasis-free Survival; LRFS, local recurrence-free survival; OS, overall survival
Immunoexpression of PSAT1 in benign nasopharyngeal epithelial tissue (A), low-stage (B), and high-stage (C) nasopharyngeal carcinomas, respectively. Immunohistochemically, PSAT1 expression was barely detected in benign nasopharyngeal epithelial tissue and low-stage nasopharyngeal carcinoma, but it significantly upregulated in high-stage nasopharyngeal carcinoma
Log-rank test revealed that PSAT1 overexpression was predictive of poor prognosis, including disease-specific survival, distant metastasis-free survival, local recurrence-free survival, and overall survival.
The regulatory mechanism of PSAT1 expression remains largely unknown. But it has been reported that MicroRNA (MiR)-340, playing a role in tumor suppression in esophageal squamous cell carcinoma, inhibits tumor proliferation via targeting of PSAT1, and PSAT1. In this manner, MiR-340 is involved in cancer cell proliferation and invasion in esophageal squamous cell carcinoma, suggesting a possible regulatory mechanism of PSAT1 expression30. Few if any previous reports have disclosed the role of PSAT1 in regulating cell proliferation. It is interesting that PSAT1 is overexpressed in non-small cell lung cancer, and it is involved in tumor cell proliferation and cell cycle progression. PSAT1 enhances G1 activity via modulation of cyclin D1 degradation and Rb-E2F pathway activity, suggesting its unique intracellular signaling axis31.
Our study found that high PSAT1 expression was a potent prognostic factor for DSS, DMeFS, LRFS and OS in NPC patients. The identification of biomarkers that independently correlate with tumor aggressiveness is important for the individualized management of high risk NPC. We confirmed increased hazard ratios of DSS, DMeFS, LRFS and OS in NPC patients with advanced stages (III-IV). A significant association between PSAT1 expression, primary tumor size, nodal status and AJCC stage of NPC was observed. Therefore, we hypothesized that high PSAT1 expression may represent NPC progression via an amino acid biosynthetic process.
PSAT1 overexpression in colon and breast cancers correlates with advanced tumor stage, chemoresistance and poor prognosis to endocrine therapy28. A high expression level of PSAT1 was associated with an advanced stage of NPC and poor prognosis compared to the NPC patients with low PSAT1 expression in our study. The role of PSAT1 in tumorigenesis and NPC development and progression and the use of PSAT1 as a treatment target require further investigation.
In conclusion, PSAT1 was overexpressed in the transcriptome of NPC, and NPC protein was identified in NPC tissue using immunohistochemistry. PSAT1 was associated with advanced tumor stage, and it independently predicted a poor prognosis of NPC.
The authors have declared that no competing interest exists.
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Corresponding author: Chien-Feng Li, M.D., Ph.D., Division of Clinical Pathology, Chi Mei Medical Center, 901 Chunghwa Road, Yung Kang Dist., Tainan County 710, TAIWAN, Tel: +886-6-2812811 ext. 53680, Fax: +886-6-2511235, E-mail: angelo.pcom.tw.