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Comparison of hepatic and serum lipid signatures in hepatocellular carcinoma patients leads to the discovery of diagnostic and prognostic biomarkers

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Oncotarget. 2018; 9:5032-5043. https://doi.org/10.18632/oncotarget.23494

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Yonghai Lu, Juanjuan Chen, Chong Huang, Ning Li, Li Zou, Sin Eng Chia, Shengsen Chen, Kangkang Yu, Qingxia Ling, Qi Cheng, Mengqi Zhu, Weidong Zhang, Mingquan Chen and Choon Nam Ong _

Abstract

Yonghai Lu1,2,*, Juanjuan Chen3,*, Chong Huang4, Ning Li4, Li Zou1, Sin Eng Chia1, Shengsen Chen4, Kangkang Yu4, Qingxia Ling4, Qi Cheng4, Mengqi Zhu4, Weidong Zhang5, Mingquan Chen4 and Choon Nam Ong1,6

1Saw Swee Hock School of Public Health, National University of Singapore, Singapore

2Institute of Nutrition and Health, Qingdao University, Qingdao, Shandong, China

3School of Marine Science, Ningbo University, Ningbo, Zhejiang, China

4Department of Infectious Diseases and Hepatology of Huashan Hospital, Fudan University, Shanghai, China

5School of Pharmacy, Second Military Medical University, Shanghai, China

6NUS Environmental Research Institute, National University of Singapore, Singapore

*These authors contributed equally to this work

Correspondence to:

Choon Nam Ong, email: ephocn@nus.edu.sg

Mingquan Chen, email: mingquanchen@fudan.edu.cn

Keywords: lipidomics, mass spectrometry, hepatocellular carcinoma, liver tissue, serum

Received: June 22, 2017     Accepted: September 03, 2017     Published: December 13, 2017

ABSTRACT

We compared hepatic and serum lipid changes in hepatocellular carcinoma (HCC) patients to have a better understanding of the molecular pathogenesis of this disease and discovery novel lipid biomarkers. Hepatic and serum lipid profiling was conducted in paired liver and serum samples from 50 HCC patients and 24 healthy controls. A total of 20 hepatic and 40 serum lipid signatures were identified, yet there was hardly any significant correlation between them. The results indicated that triglycerides and phosphatidylcholines contributed significantly to altered hepatic lipids, whereas triglycerides and phosphatidylethanolamine-based plasmalogens (PEp) contributed most to altered serum lipids. In serum, PEp (36:4) and (40:6) showed a fair capability to discriminate HCC patients from healthy controls, and were significantly associated with HCC tumor grades (p < 0.05), and thus were identified as potential diagnostic and prognostic biomarkers of HCC. These findings were confirmed by a validation study conducted in an independent cohort consisting of 18 HCC, 20 cirrhosis patients, and 20 healthy controls. This study suggests that hepatic and serum lipid signatures of HCC have to be considered as mostly independent, and the results imply potential roles of PEp species, particularly PEp (36:4) and (40:6), as serum biomarkers for HCC diagnosis and progression.


Comparison of hepatic and serum lipid signatures in hepatocellular carcinoma patients leads to the discovery of diagnostic and prognostic biomarkers | Lu | Oncotarget

INTRODUCTION

Hepatocellular carcinoma (HCC) is one of the most frequently encountering malignancies, marked by a poor 5-year survival rate of less than 5%. In addressing the demands for molecular diagnosis and therapy of HCC, extensive efforts have been made in the last two decades to identify altered expressed genes by genomics, proteins by proteomics, and metabolites by metabolomics in HCC patients [16]. In addition, it is worth noting that numerous lipid changes in HCC patients were reported in metabolomics studies [614].

Lipids are a group of naturally occurring hydrophobic molecules that play important roles in biological functions by storing energy, signaling, and acting as structural components of cell membranes [15]. Recent advances in lipidomics provided a new angle for lipid investigation in cancer research [1622]. Yet to date, however, only a few lipidomics studies have been carried out to characterize hepatic [2325] and serum [26, 27] lipid profiles of HCC patients. Previous studies showed the increase of phosphatidylcholines (PCs) [23] and the reduction of phosphatidylethanolamines (PEs), phosphatidylserines (PSs) and phosphatidylinositols (PIs) [25] in HCC tumors. In serum, most lipids were found to be diminished in HCC patients compared to healthy controls and hepatitis patients, including PCs, sphingomyelins (SMs), triglycerides (TGs), and cholesterol esters (CEs) [26]. Building on these findings, our current knowledge of the aberrant lipid metabolism in HCC is still in its infancy, leaving much of the fundamental aspects of their biology unknown. Additionally, the relationship between hepatic and serum lipid changes in HCC patients remains unclear. Liver plays a key role in lipid metabolism, including synthesis of lipoproteins and intracellular catabolism of lipids [28]. The aberrant lipid metabolism in liver may provide first-hand information on the development of liver diseases. Blood serum is a readily accessible and widely used homeostatic biofluid in clinic tests, providing information in regard to an individual’s physiological status [29]. Therefore, better understanding of the correlation between hepatic and serum lipid changes could improve the molecular characterization of HCC and help to identify disease-relevant biomarkers.

In this study, we characterized both hepatic and serum lipid profiles of 50 HCC patients using an untargeted lipidomics approach. When examining the lipid profiles, we aimed to compare the hepatic and serum lipid signatures in HCC patients, and also intended to identify the specific lipid biomarkers that could be used for diagnosis and progression of HCC.

RESULTS

Demographic and clinical characteristics of subjects

A total of 74 and 58 participants were respectively recruited from two study sites in this study, and their characteristics are shown in Table 1 and Supplementary Table 1. There were no significant differences on age and gender between groups in each batch. HCC patients had higher α-fetoprotein (AFP) levels than liver cirrhosis patients (p < 0.05) (Supplementary Table 1), and among HCC patients those who have cirrhosis also had higher AFP levels than those who do not have (Supplementary Table 2). Meanwhile, it was found that up to 40% (20 out of 50, Table 1) HCC patients had normal AF P values (i.e., < 20 mg/L) [30]. No significant differences were observed on alanine transaminase (ALT), aspartate transaminase (AST), and gamma-glutamyl transpeptidase (GGT) were found between HCC and liver cirrhosis patients (Supplementary Table 1), and between HCC patients with and without liver cirrhosis (Supplementary Table 2).

Table 1: Characteristics of 50 hepatocellular carcinoma (HCC) patients and 24 healthy individuals

Characteristics a

HCC patients

Healthy individuals

P values b

No. of subjects

50

24

Gender (M/F)

38/12

19/5

0.766

Age (year)

53 (34~72)

55 (24~64)

0.706

AFP (mg/L)

45.3 (1.62~24200)

-

 > 20/< 20

30/20

ALT (U/L)

54 (17~695)

-

AST (U/L)

63.5 (20~903)

-

GGT (U/L)

86.5 (11~647)

-

HBsAg (positive/negative)

46/4

0/24

HCVAb (positive/negative)

1/49

0/24

Cirrhosis/no cirrhosis

29/21

TNM stages

 T1N0M0 (early-stage)

12

 T2N0M0 (early-stage)

19

 T3N0M0 (late-stage)

10

 T4N0M0 (late-stage)

9

a Age, AFP, ALT, AST, and GGT in HCC patients were expressed as median (range). Limitation on the number of subjects, T1 and T2 were set as early-stage of HCC; T3 and T4 were set as late-stage of HCC.

b Chi-square test for gender, and Student’s t-test for age.

Hepatic and serum lipid signatures in HCC patients

We started our investigation using a principal component analysis (PCA) model to explore the variances of lipid profiles among the three types of liver tissues. As illustrated in the score scatter plot (Supplementary Figure 1), hepatocellular carcinoma tissue (HCT) samples were separated from adjacent noncancerous tissue (ANT) and distal noncancerous tissue (DNT) samples with a few overlaps, while there was no significant separation between ANT and DNT samples. Besides, we compared the lipid profiles between two respective groups among these three types of liver tissues, respectively. All the results demonstrated that lipid profiles were not significantly different between ANT and DNT samples. Thus, we focused on the differences between HCT and DNT samples to investigate hepatic lipid signatures of HCC. As previous report [6], orthogonal partial least-squares discriminant analysis (OPLS-DA) was applied to rank all lipids with respect to their performance for discriminating between HCT and DNT (Figure 1A). Finally, 20 lipid signatures were identified in HCC tumors, including six TGs, three PCs, three PEs, two phosphatidylglycerols (PGs), two PIs, two PSs, one SM, and one CE (Table 2). Their relative average quantities in HCT and DNT samples are shown in a heat map using MeV software (Supplementary Figure 2). Furthermore, OPLS-DA was applied to explore serum lipid signatures (Figure 1B). Finally, 40 lipid signatures were identified in serum, including 19 TGs, three lysophosphatidylcholines (LPCs), three PCs, eight PEs, one PI, three ceramides (Cers), one SM, and two CEs (Table 3). The relative average quantities of lipids in HCC patients and healthy controls are shown in Supplementary Figure 3. Stratification by cirrhosis status in HCC patients indicated that cirrhosis had no significant effects on the expression of most lipids in HCC patients (Supplementary Tables 3 and 4). On the basis of KEGG PATHWAY Database (http://www.genome.jp/kegg/) and literature, a map of HCC related lipid network was established based on these lipid signatures (Supplementary Figure 4).

Figure 1:

Figure 1: OPLS-DA score scatter plots show perturbations of hepatic (A) and serum (B) lipid profiles in hepatocellular carcinoma (HCC) patients.

Table 2: The 20 lipid signatures identified in the liver samples

Lipids

Candidates a

R.T. (min)

m/z

Fragments

Formula

Trend b

[M+H]+

[M+NH4]+

[M-H]-

Glycerolipids

TG(51:0)

TG(16:0/17:0/18:0) [iso6]

15.96

866.8201

593, 579, 565, 267, 253, 239

C54H104O6

Up

TG(53:1)

TG(16:0/18:1/19:0) [iso6]

16.04

892.8365

619, 593, 577, 281, 265, 239

C56H106O6

Up

TG(55:2)

TG(15:0/18:1/22:1) [iso6]

16.12

918.8533

645, 619, 563, 321, 265, 225

C58H108O6

Up

TG(56:1)

TG(16:0/18:1/22:0) [iso6]

19.54

934.8825

661, 635, 577, 323, 265, 239

C59H112O6

Up

TG(58:1)

TG(16:0/18:1/24:0) [iso6]

22.98

962.9139

689, 663, 577, 351, 265, 239

C61H116O6

Up

TG(60:2)

TG(16:0/18:1/26:1) [iso6]

22.97

988.9299

715, 689, 577, 377, 265, 239

C63H118O6

Up

Glycerophospholipids

PC(28:0)

PC(14:0/14:0)

6.69

678.5098

619, 468, 184

C36H72NO8P

Up

PC(31:0)

PC(15:0/16:0) [iso2]

7.89

720.5581

661, 494, 480, 184

C39H78NO8P

Up

PC(35:0)

PC(17:0/18:0) [iso2]

9.27

776.6212

717, 522, 508, 184

C43H86NO8P

Up

PE(34:2)

PE(16:0/18:2) [iso2]

7.61

714.5101

279, 255, 196

C39H74NO8P

Down

PE(38:6)

PE(16:0/22:6) [iso2]

7.38

762.5107

327, 255, 196

C43H74NO8P

Down

PE(40:6)

PE(18:0/22:6) [iso2]

8.06

790.5404

327, 283, 196

C45H78NO8P

Down

PG(36:3)

PG(18:1/18:2) [iso2]

6.51

771.5208

697, 281, 279, 153

C42H77O10P

Down

PG(36:4)

PG(18:2/18:2)

5.99

769.5057

695, 279, 153

C42H75O10P

Down

PI(34:2)

PI(16:0/18:2) [iso2]

6.63

833.5204

577, 553, 279, 255, 153

C43H79O13P

Down

PI(36:2)

PI(18:0/18:2) [iso2]

7.32

861.5523

581, 577, 283, 279, 153

C45H83O13P

Down

PS(38:6)

PS(16:0/22:6) [iso2]

6.83

806.4950

719, 327, 255, 153

C44H74NO10P

Down

PS(40:6)

PS(18:0/22:6) [iso2]

7.47

834.5307

747, 327, 283, 153

C46H78NO10P

Down

Sphingolipids

SM(d34:2)

SM(d18:1/16:1)

6.75

701.5615

683, 184

C39H77N2O6P

Up

Sterol lipids

CE(22:6)

11.75

714.6216

369

C49H76O2

Up

a [iso6] means that the lipid might have six candidates/isomers, further analysis is needed for structure identification. Similar means for [iso2].

b “Up” and “Down” represent the lipid is up- and down-regulated in HCC tumor tissues compared to matched normal tissues, respectively.

Table 3: The 40 lipid signatures identified in the serum samples

a [iso6] means that the lipid might have six candidates/isomers, further analysis is needed for structure identification. Similar means for [iso3] and [iso2].

b “Up” and “Down” represent the lipid is up- and down-regulated in serum of HCC patients compared to health individuals, respectively.

c AUC value of ROC analysis between HCC patients and healthy subjects.

Comparison of hepatic and serum lipid signatures

Among the hepatic and serum lipid signatures, only three lipids were common between them, they are PE (38:6), (40:6), and CE (22:6). Among them, PE (38:6) and (40:6) showed the same change trend in liver and serum, but CE (22:6) showed an opposite trend. Although TGs, PCs, PIs, SMs and CEs were changed in both liver and serum, these lipid species showed opposite trends. In addition, there was hardly any significant correlation between hepatic and serum lipid signatures in HCC patients (Supplementary Figure 5). These observations suggested that hepatic and serum lipid changes of HCC are rather difference and independent. With factor analysis (Table 4), it was found that TGs (factor 1) and PCs (factors 1 and 2) contributed most significantly towards the altered hepatic lipid metabolism in HCC patients, whereas TGs (factor 1) and phosphatidylethanolamine-based plasmalogens (PEp) (factor 2) contributed most significantly to the altered serum lipid metabolism.

Table 4: Percentage of variances and main loadings (loading value > 0.5) explained by first two factors for hepatic and serum lipid changes in hepatocellular carcinoma (HCC) patients

% of Variance

Liver

Serum

Factor 1 (31.8%)

Factor 2 (14.6%)

Factor 1 (36.6%)

Factor 2 (14.9%)

Main Loadings

TG(51:0)

PC(31:0)

TG(46:3)

PEp(36:4)

TG(53:1)

PE(40:6)

TG(48:0)

PEp(38:4)

TG(55:2)

PS(40:6)

TG(48:1)

PEp(38:6)

TG(56:1)

TG(48:2)

PEp(40:6)

TG(58:1)

TG(48:3)

PEp(40:7)

TG(60:2)

TG(49:1)

PC(40:7)

PC(28:0)

TG(50:0)

PC(35:0)

TG(51:1)

TG(52:0)

TG(52:1)

TG(53:1)

TG(53:2)

Diagnostic and prognostic capabilities of serum lipid signatures

Receiver operating characteristic (ROC) analysis indicated that 24 out of 40 serum lipids showed a fair capability in diagnostic tests, with area under the curve (AUC) scores greater than 0.8 (Table 3). Of these, we found that PEp (36:4) and (40:6) showed a gradually decreased trend with the progression of HCC from early- to late-stages (Figure 2A), and their levels were associated with TNM tumor stage (p < 0.05) (Supplementary Table 5). Although our data showed that HCC patients with cirrhosis had lower levels of PEp (36:4) and (40:6) than those without cirrhosis (p < 0.05) (Supplementary Table 4), the decreased trend of these two lipids from early- to late-stages were not affected by the cirrhosis status, as the frequency of HCC patients suffering from cirrhosis was similar in the two stage groups, 60% and 58% respectively. Furthermore, a classification with AUC equal to 0.880 was achieved when using the two lipids together to classify HCC patients and healthy subjects (Figure 2B). Our results tend to suggest that PEp (36:4) and (40:6) appear to be potential serum biomarkers for diagnosis and progression of HCC.

Diagnostic capabilities of PEp (36:4) and (40:6) for hepatocellular carcinoma (HCC).

Figure 2: Diagnostic capabilities of PEp (36:4) and (40:6) for hepatocellular carcinoma (HCC). (A) Altered expressions of PEp (36:4) and (40:6) in serum of healthy subjects, early-stage HCC patients, and late-stage HCC patients; (B) ROC curve of serum PEp (36:4) and (40:6) in the discovery set; (C) Altered expressions of PEp (36:4) and (40:6) in serum of healthy subjects, liver cirrhosis patients, and HCC patients; (D) ROC curve of the combination of PEp (36:4) and (40:6) in the validation set; (E) Discrimination of healthy subjects, liver cirrhosis patients, and HCC patients by using the combined serum levels of PEp (36:4) and (40:6), at a cut-off of probability of 0.5; (F) Diagnostic accuracy of the combined marker PEp (36:4) and (40:6) for HCC patients with different concentrations of AFP in the validation set.

External validation

A semi-quantitative analysis of PEp (36:4) and (40:6) were carried out in the validation set to verify their capabilities for diagnosis and progression of HCC. Their levels were found to be significantly reduced in HCC and liver cirrhosis patients compared to healthy individuals, as well as their levels in HCC patients were much lower than those in liver cirrhosis patients (Figure 2C). Diagnostic tests showed that a combination of PEp (36:4) and (40:6) had good potential to discriminate HCC patients from both healthy individuals (AUC = 0.946) and liver cirrhosis patients (AUC = 0.732) (Figure 2D). Further, the c-statistic was increased from 0.732 in the basic model to 0.772 when putting AFP levels in the prediction model to differentiate HCC patients from liver cirrhosis patients (Supplementary Figure 6). The prediction probability values of the combined marker on HCC are shown in Figure 2E. At the cut-off value of 0.5 [31], 17 out of 18 HCC patients were correctly classified when compared to healthy individuals, giving a sensitivity of 89% and a specificity of 95%; 13 were correctly classified when compared to liver cirrhosis patients, giving a sensitivity of 62% and a specificity of 71%. It is worthy to note that the combination showed 80–90% diagnostic accuracy in these HCC patients with normal AF P values (< 20 ng/mL) (Figure 2F). Owing to the small samples size of HCC patients, we did not observer the significant association between PEp (36:4) and (40:6) levels with HCC tumor grade in the validation set (Supplementary Table 6), yet they still showed a gradually decreased trend (Supplementary Figure 7).

DISCUSSION

In order to reveal the relationship between hepatic and serum lipid changes in HCC, we first characterized both hepatic and serum lipid profiles of 50 HCC patients and went further to identify the differential lipids. A total of 20 hepatic and 40 serum lipid signatures were identified in HCC patients, covering a wide range of lipid species including TGs, LPCs, PCs, PEs, PGs, PIs, PSs, Cers, SMs, and CEs. We noted that lipid metabolism in HCC tumors and sera are likely to be modulated in different manners, as most lipid species showed opposite tendency of changes in liver and serum, and only a few hepatic and serum lipids shared moderate correlations. Factor analysis confirmed that the altered hepatic lipid metabolism in HCC was mainly driven by TGs and PCs; the altered serum lipid metabolism was mainly driven by TG and PEp species.

Increased de novo lipogenesis is a common feature to most solid tumors, which occurs in tumourigenesis to supply energy and membrane lipids for accelerated cell proliferation [32]. TG is a precursor for synthesis of phospholipids, and also is a primary unit of energy storage [26], which is synthesized in liver beginning with acylation of glycerol-3-phosphate catalyzed by lysophosphatidic acid (LPA)-acyltransferase [33]. A recent study indicated that the isoleucine to methionine substitution at position 148 on patatin-like phospholipase domain-containing 3 (PNPLA3, adiponutrin) gene induced a gain of function in LPA-acyltransferase activity, leading to increased hepatic TG biosynthesis in HCC patients [34]. In addition, our previous study indicated that glycerol-3-phosphate significantly decreased in HCC tumors [6]. Taking them together, our current finding that TGs significantly increased in HCC tumors might be caused by the increased flux of glycerol-3-phosphate to TG in cancer cells. Besides de novo TG synthesis, HCC tumors also scavenge lipids from their environment. Previous study had indicated that uptake of fatty acids by cancer cells plays an important role in the development and progression of HCC [35]. Thus, enhanced TG uptake by HCC cancer cells from serum may also contribute to the increased TG levels in HCC tumors. It could also help explain why TG species reduced in serum of HCC patients as observed in our study and previous report [26], but further investigations are required to confirm these observations. Nevertheless, our study indicated an increase in TG synthesis/uptake in HCC tumors (Supplementary Figure 4).

Further, a series of glycerophospholipids were found to be altered significantly in HCC patients, including PCs, PEs, PGs, PIs, and PSs. Among them, PC and PE account for 40–60% of phospholipids of eukaryotic membranes and play important roles in cellular structure and biological functions [36]. A recent study showed that overexpression of LPC acyltransferase 1 enriched PC species in HCC tumors and promoted cell proliferation, which catalyzes the conversion of LPC to PC in the Lands cycle pathway of PC biosynthesis [24], which supports our finding that the elevated PC species in HCC tumors. In addition, we found that PC species were significantly decreased in serum of HCC patients, which was consistent with previous study as well [26]. In this study, five plasmalogens were found to be significantly reduced in serum of HCC patients compared to healthy controls, including PEp (36:4), (38:4), (38:6), (40:6) and (40:7). Plasmalogens are a type of ether phospholipids characterized by fatty alcohols with a vinyl ether linkage at sn-1 position and polyunsaturated fatty acids (PUFAs) with an ester linkage at sn-2 position. Although functions of plasmalogens have not yet been fully elucidated, it has been reported that they can reduce the damaging effects of reactive oxygen species in cancer cells [37]. To date, serum plasmalogen deficiencies have been linked to several cancers (e.g., colon cancer, prostate cancer, lung cancer, breast cancer, ovary cancer, and kidney cancer) [38].

Another important feature observed in HCC patients was the significant reduction of docosahexaenoic acid (DHA)-content glycerophospholipids, including LPC (22:6), PC (40:7), (40:9), PE (38:6), (40:6), PEp (38:6), (40:6), (40:7), and PS (38:6), (40:6) (Table 2 and 3). DHA is an omega-3 PUFA, which can be synthesized from alpha-linolenic acid, but mostly obtained directly from the diet. In 2009, Lim et al. found that omega-3 PUFAs such as DHA and eicosapentaenoic acid (EPA) could inhibit HCC cancer cell growth by blocking β-catenin and cyclooxygenase-2 [39]. The reduction of DHA-content glycerophospholipids observed in our study might be because of self-protection consumption, in which DHA was released from glycerophospholipids for self-care intervention. It is worth noting that our previous study also indicated a reduction in PUFAs (e.g., linoleic acid) in HCC tumors [6].

Ideally, the biomarkers used for disease diagnosis and progression should be easily accessible in clinical tests. Therefore, we only investigated the diagnostic and prognostic potential of serum lipid signatures for HCC. Although TGs, particularly TG (50:0), (52:0) and (52:1), showed the highest potential in the diagnosis of HCC with AUC > 0.9, their changes were not associated with the progression of HCC. Conversely, we found that the changes of PEp (36:4) and (40:6) were significantly correlated with TNM tumor grade (p < 0.05), and they also showed a moderate potential for HCC diagnosis (AUC >0.8). In this study, we aimed to find the lipid biomarkers with both diagnostic and prognostic capabilities, and thus we focused on the changes of PEp (36:4) and (40:6) in the validation study. The results confirmed that the two lipids could differentiate HCC patients form liver cirrhosis patients and healthy subjects with high sensitivity and specificity (Figure 2E). More importantly, they showed high diagnostic accuracy for HCC patients with low AF P values, providing a supplementary role to AFP for HCC diagnosis (Figure 2F).

The strengths of this study include the use of paired liver and serum samples and a well-established MS technique. This study is among the first to investigate the correlation between hepatic and serum lipid changes in HCC patients using an untargeted lipidomics method. Here, some limitations of our study still need to be acknowledged. First, the validation study was conducted within a limited number of participants. Further, in the validation phase, PEp (36:4) and (40:6) were only semi-quantitative because of no available standards. Therefore, the two candidate biomarkers from this study should be validated in a large replication cohort using standards.

In summary, a wide range of hepatic and serum lipid signatures was identified in HCC patients, including TGs, LPCs, PCs, PEs, PGs, PIs, PSs, Cers, SMs, and CEs. Compared with the limited lipid studies of HCC, our results indicated that hepatic and serum lipid changes in HCC patients might be modulated in different manners. The overall data indicated that PEp (36:4) and (40:6) showed significant diagnostic potential for HCC, and their levels were associated with TNM tumor grade. External validation verified that they are two candidate diagnostic biomarkers of HCC, while their potential roles as prognostic biomarkers of HCC need to be investigated further.

MATERIALS AND METHODS

Participants and sample collection

A batch of 50 HCC patients and 24 healthy volunteers were recruited at the Shanghai Huashan Hospital (Shanghai, China) between February 2011 and August 2012 (Table 1). Due to the limitation of subject numbers, 50 HCC patients were simply classified into early- and late-stages according to TNM staging system for progression investigation of HCC, in which T1 and T2 were set as early-stage of HCC (n = 31); T3 and T4 were set as late-stage of HCC (n = 19). Of these, 46 HCC patients were hepatitis B surface antigen (HBsAg) positive, and one was anti-hepatitis C virus (HCV) positive. Hepatic lipid profiling of 50 HCC patients was conducted by using a pairwise comparison of HCC tumor tissues and matched normal liver tissues of each patient. Three types of liver tissue were collected as surgical specimens from each HCC patient during surgery: HCT was from the central area of the solid tumor, ANT was collected at 1–2 cm surrounding the solid tumor, and DNT was collected at 5 cm away from the solid tumor. The tissue samples were snap-frozen with liquid nitrogen followed by storage at –80°C until analysis. Serum lipid profiling of 50 HCC patients was carried out by comparison with the 24 healthy subjects. The morning fasting antecubital venous blood samples were collected from the participants using a sterile 21-gage needle syringe, allowed to clot at 4°C overnight and centrifuged at 1,699 g for 10 min to obtain sera. The serum samples were stored in Eppendorf micro-tubes at –80°C until analysis. These 150 liver tissue and 74 serum samples were used as a discovery set for the identification of potential lipid signatures. The lipid signatures with diagnostic and prognostic potential were further evaluated in an independent batch of 58 serum samples from 18 HCC patients, 20 liver cirrhosis patients, and 20 healthy individuals, as described in the Supplemental Materials and Methods. The 58 subjects were recruited at the Jurong People’s Hospital (Jiangsu, China) between April 2013 and June 2014 (Supplementary Table 1). Among them, 15 HCC and 14 liver cirrhosis patients were HBsAg positive, and 3 HCC and 6 liver cirrhosis patients were anti-HCV positive. All participants voluntarily joined this study, gave written informed consent, and completed a questionnaire that provided demographical information including age, gender, lifestyle factors, and medical family history. The study protocols were approved by the Institutional Review Boards at the Huashan Hospital, Jurong People’s Hospital and National University of Singapore, and conducted in accordance with the Helsinki Declaration of 1975, as revised in 1996.

Sample preparation

Tissue extraction was performed using a modified method to that described by Roberts et al. [40]. Frozen liver tissue (5 ± 0.05 mg) was mixed with 400 μL of chloroform/methanol (2:1, v/v) containing 2.5 μg/mL PC (15:0) and 5 μg/mL PC (17:0/17:0) as internal standards. The mixture was homogenized using a TissueLyser LT (Qiagen, UK) at 25 Hz for 10 min, then sonicated for 15 minutes. Following this, 200 μL of chloroform and 200 μL of water were added, then centrifuged for 10 minutes at 20,187 g. The organic phase was collected and filtered by Thermo Scientific™ national 750μL micro-centrifugal filters (PTFE membrane, 0.2 μm pore size, non-sterile). The filtrate was dried under nitrogen gas, then reconstituted in 200μL chloroform/methanol (2:1, v/v) for LC-MS analysis. Serum lipids were extracted using Bligh & Dyer’s method [41] with minor modifications. Serum (100 μL) was diluted with 900 μL of chloroform/methanol/water (2:1:1, v/v/v) containing 2.5 μg/mL PC (15:0) and 5 μg/mL PC (17:0/17:0) as internal standards. The mixture was shaken vigorously for 5 min, and then centrifuged for 20 minutes at 20,187 g. The organic phase was collected and dried under nitrogen gas. The dry residues were reconstituted in 200 μL chloroform/methanol (2:1, v/v) for LC-MS analysis. Quality control (QC) samples were separately prepared for tissue and serum samples, and analyzed to evaluate the stability and reproducibility of LC-MS analytical system (Supplementary Figure 8).

LC-MS analysis

Lipid profiling was performed on an Agilent 1290 ultrahigh pressure LC system (Waldbronn, Germany) coupled to a 6540 Q-ToF mass spectrometer equipped with an electrospray ionization (ESI) source. The samples were analyzed in both ESI-positive and -negative ion modes. The separation was performed on a phenomenex Kinetex C18 column (50 × 2.1 mm, 2.6 μm) at 40°C. The mobile phases were methanol/acetonitrile/isopropyl alcohol (9:4:2, v/v/v) with 20mM HCOONH4 (A) and water/isopropyl alcohol (13:2, v/v) with 20mM HCOONH4 (B). The gradient program was: 0–5 min, 60–85% A; 5–10 min, 85–100% A; 10–25 min, 100% A; 25–26 min, 100–60% A. The flow rate was set at 0.4 mL/min. A 10 μL of sample was loaded for each individual analysis. Mass data were acquired between m/z 100 and 1200 at a rate of two scans per second. The ion spray voltage was set at 4,000V, and the heated capillary temperature was maintained at 350°C. The drying gas and nebulizer nitrogen gas flow rates were 12.0 L/min and 50 psi, respectively. MS/MS analysis was carried out for the identification and characterization of lipid candidates with multiple collision energies, including 10, 20 and 40 V. Lipid identifications were conducted by searching the MS/MS data against entries in the Lipid MAPS (http://www.lipidmaps.org/) and METLIN (http://metlin.scripps.edu/) databases with mass errors of < 5 ppm. We named lipid species as combined the number of carbons and the number of double bonds, as well as the candidate isomers. A workflow of manual identification of lipids used in this study is shown in Supplementary Figure 9.

Data pre-processing and statistical analysis

The hepatic and serum spectral data were exported as mzData files, and respectively pretreated by open-source software MZmine version 2.8 for peak detection, peak alignment and peak area normalization, in which the data of each sample was normalized to total area to correct for the MS response shift from the first injection to the last injection. The preprocessed lipid data were screened by using “80% rule” and missing values (i.e., zeros) were replaced by 1/2 minimum [42, 43] before statistical analysis. Analytical reliability of LC-MS method was assessed by a PCA model. The differential hepatic lipids in HCC patients were screened by comparing HCT and DNT samples. The lipids with variable importance in the projection (VIP) values of > 1.0 in the orthogonal partial least squares discriminant analysis (OPLS-DA) model and p values of < 0.05 in the paired t test were considered as signatures. Serum lipid signatures in HCC patients were defined by VI P values of > 1.0 in the OPLS-DA model and p values of < 0.05 in the Student’s t test when compared to healthy subjects. Pearson correlation analysis were performed to reveal the significant correlation between hepatic and serum lipid changes. Factor analysis was applied to reduce dimensions of lipidomics data. ROC analysis was used to evaluate the diagnostic potential of lipids. SIMCA-P 14.0 software was used for multivariate statistical analyses (PCA and OPLS-DA). The paired t test, Student’s t test, Pearson correlation analysis, factor analysis and ROC analysis were performed in IBM SPSS Statistics 24 software. P < 0.05 was considered significant. The false discovery rate method of Benjamini and Yekutieli was used to correct for multiple hypothesis testing & reduce false positives.

Abbreviations

HCC: hepatocellular carcinoma; PCs: phosphatidylcholines; PEs: phosphatidylethanolamines; PSs: phosphatidylserines; PIs: phosphatidylinositols; SMs: sphingomyelins, TGs: triglycerides; CEs: cholesteryl esters; AFP: alpha-fetoprotein; ALT: alanine transaminase; AST: aspartate transaminase; GGT: gamma-glutamyl transpeptidase; PCA: principal component analysis; HCT: hepatocellular carcinoma tissue; ANT: adjacent noncancerous tissue; DNT: distal noncancerous tissue; OPLS-DA: orthogonal partial least-squares discriminant analysis; PGs: phosphatidylglycerols; LPCs: lysophosphatidylcholines; Cers: ceramides; PEp: phosphatidylethanolamine-based plasmalogens; ROC: receiver operating characteristic; AUC: area under the curve; LPA: lysophosphatidic acid; PNPLA3: patatin-like phospholipase domain-containing 3; PUFAs: polyunsaturated fatty acids; DHA: docosahexaenoic acid; EPA: eicosapentaenoic acid; HBsAg: hepatitis B surface antigen; HCV: hepatitis C virus; QC: quality control; ESI: electrospray ionization; VIP: variable importance in the projection.

ACKNOWLEDGMENTS AND FUNDING

This study was partially supported by the grant of Natural Science Fund of The Science and Technology Commission of Shanghai, China (12ZR1404300), Science and Technology Commission of Shanghai Municipality (16411954300), NUS secondment Funds to CNO (706-000-005-133) and NUS Environmental Research Institute (NERI) (608-000-007-731). The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

CONFLICTS OF INTEREST

The authors have no conflicts of interest to declare.

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