Circulating Tumor Cells Undergoing the Epithelial–Mesenchymal Transition: Influence on Prognosis in Cytokeratin 19-Positive Hepatocellular Carcinoma
Authors Zhang Q, Xing W, Zhang J, Hu J, Qi L, Xiang B
Received 22 December 2020
Accepted for publication 15 February 2021
Published 2 March 2021 Volume 2021:14 Pages 1543—1552
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 2
Editor who approved publication: Dr Federico Perche
Qian Zhang,1,2,* Wanting Xing,1,2,* Jie Zhang,1,2 Junwen Hu,1,2 Lunan Qi,1– 3 Bangde Xiang1– 3
1Department of Hepatobiliary Surgery, Guangxi Medical University Cancer Hospital, Nanning, People’s Republic of China; 2Key Laboratory of Early Prevention and Treatment for Regional High Frequency Tumors, Ministry of Education, Nanning, People’s Republic of China; 3Guangxi Liver Cancer Diagnosis and Treatment Engineering and Technology Research Center, Nanning, People’s Republic of China
*These authors contributed equally to this work
Correspondence: Bangde Xiang; Lunan Qi
Department of Hepatobiliary Surgery, Guangxi Medical University Cancer Hospital, 71# Hedi Road, Qingxiu District, Nanning, Guangxi, 530021, People’s Republic of China
Tel +86-7715301253; +86-13517886990
Email [email protected]; [email protected]
Purpose: The purpose of this study was to elucidate the relationship between cytokeratin 19 (CK19) expression and levels of circulating tumor cells (CTCs) in preoperative peripheral blood of patients with hepatocellular carcinoma (HCC), and the potential influence of that relationship on prognosis.
Patients and Methods: CanPatrol™ CTC-enrichment technique and in situ hybridization (ISH) were used to enrich and classify CTCs undergoing the epithelial–mesenchymal transition (EMT) from blood samples of 105 HCC patients. CK19 immunohistochemistry staining was performed on HCC tissues and compared with demographic and clinical data.
Results: In total, 27 of 105 (25.7%) HCC patients were CK19-positive. CK19-positive patients had significantly lower median tumor-free survival (TFS) than CK19-negative patients (5 vs 10 months, P = 0.047). In total, 98 (93.3%) patients showed pre-surgery peripheral blood CTCs (range: 0– 76, median: 6), and 57 of 105 (54.3%) patients displayed CTC counts ≥ 6. Furthermore, CK19-positive patients with CTC count ≥ 6 showed significantly higher percentage than CK19-negative ones (77.8% vs 46.2%, P = 0.004). CK19-positive patients showed a significantly higher proportion of mesenchymal CTCs among CTCs undergoing EMT than CK19-negative patients (mean rank: 62.28 vs 49.79, P = 0.046). We also found that CK19-positive patients with high CTC count showed significantly shorter median tumor-free survival than CK19-negative patients with low CTC count (5 vs 16 months, P = 0.039).
Conclusion: High CTC count and high percentage of mesenchymal CTCs are closely related to the expression of CK19, which is associated with poor prognosis in HCC patients.
Keywords: hepatocellular carcinoma, cytokeratin 19, circulating tumor cells, prognosis, tumor-free survival
Hepatocellular carcinoma (HCC) is one of the most frequent cancers and the second leading cause of death in China.1,2 HCC shows several characteristics of malignant progression that are associated with poor prognosis, including fast growth, strong invasion, easy infiltration into blood vessels and spreading through blood, as well as progression through the epithelial–mesenchymal transition (EMT).3 Despite improvement in surveillance and treatment, prognosis remains poor due to the high incidence of recurrence and metastasis.4 Currently, the concept of “precision medicine” recommends treating each patient with liver cancer differently in order to maximize the chances of survival.5,6 Therefore, early diagnosis, optimization of treatment strategies and post-treatment monitoring are very important for the management and survival of HCC patients.
Conventional imaging techniques, such as computed tomography or magnetic resonance imaging, lack sensitivity for small lesions. Serum alpha-fetoprotein (AFP) is currently an important biomarker for the early screening of HCC and monitoring after treatment,7 but it can be inaccurate.8,9
A growing body of research indicates that the monitoring of circulating tumor cells (CTCs) may be useful for the diagnosis of malignant tumors, assessment of disease, selection of treatment methods, and evaluation of prognosis.10–15 In patients with breast, rectal, or lung cancer, high numbers of CTCs in peripheral blood have been associated with higher rate of postoperative recurrence and worse response to radio- and chemotherapy.11,14,16 CTCs are rare cancer cells that have escaped from the primary solid tumor and entered the circulatory system. They function as seeds for metastases and can be classified as epithelial type (E-CTC), mesenchymal type (M-CTC), or an intermediate type in transition from epithelial to mesenchymal (E/M-CTC). These subtypes can be distinguished based on expression of surface markers. E-CTCs can be transformed into M-CTCs and vice versa.17,18
In HCC, cytokeratin 19 (CK19) is a marker of hepatic progenitor cells and acts as a key player in tumor invasion, indicating poor prognosis.19,20 Over the past years, many studies have shown that CK19-positive HCC has unique biological characteristics regarding tumor stem cells, angiogenesis, invasiveness, and tumor cell apoptosis.21–25 CK19 is closely related to epithelial–mesenchymal transition (EMT), CK19-positive cells acquire mesenchymal characteristics through the EMT and strongly proliferate due to the activation of transforming growth factor beta (TGFb)/Smad signaling.26 However, the relationship between CK19 expression and CTCs in HCC is unclear.
Therefore, based on the biological characteristics of CK19-positive tumors and the process of CTCs generation, we hypothesized that CK19 may involve in EMT transformation and increase the number of CTCs, which can result in poor prognosis of HCC patients. Therefore, the aim of our study was to investigate the potential relationship between CTC levels in peripheral blood and CK19 expression in HCC patients, and assess the potential influence of this relationship on prognosis.
Patients and Methods
From March 2014 to May 2017, a total of 105 HCC patients treated with R0 resection at the Guangxi Medical University Cancer Hospital, Nanning, Guangxi Province, China, were enrolled. Flow chart of patient enrollment is shown in Figure 1. Those patients were retrospectively enrolled in the current study if they satisfied all the following inclusion criteria: (1) definitive pathological diagnosis of HCC based on the World Health Organization criteria;27 (2) Child-Pugh A stage and Performance Status Test (PST) score of 0–1; (3) no prior anticancer treatment, such as transarterial chemoembolization or radiation; and (4) R0 resection, defined as complete macroscopic removal of the tumor, negative resection margins, and no detectable intra- or extrahepatic metastatic lesions. Other relevant clinical data were obtained for each patient from medical records.
Figure 1 Flow chart of patient enrollment.Notes: The 105 patients were divided into two sub-groups based on median CTC counts: patients were classified as having low total CTC count (>6) and as having high total CTC count (≥6)
This study was conducted in accordance with the Declaration of Helsinki guidelines, and the protocol of this trial was approved by the Ethics Committee of the Tumor Hospital of Guangxi Medical University. On admission, all patients provided written consent for their medical data to be analyzed and published for research purposes.
CTC Isolation and in situ Hybridization
The CanPatrolTM system was used to isolate CTCs as previously described.28–31 Blood samples were collected 1 or 2 days before surgery. Peripheral blood samples (5 mL, anticoagulated with ethylenediaminetetraacetic acid) were collected after discarding the first 2 mL to avoid contamination with skin cells. Red blood cell lysis buffer (Sur Exam, Guangzhou, China) was used to remove erythrocytes, and the cells were resuspended in phosphate-buffered saline (PBS) with 4% formaldehyde (Sigma, St. Louis, MO, USA) for 5 min. Next, the blood was filtered using a system including a filtration tube containing a 8-μm pore membrane (Sur Exam), a manifold vacuum plate with valve settings (SurExam), an E-Z96 vacuum manifold (Omega, Norcross, GA, USA), and a vacuum pump (Auto Science, Tianjin, China). The pumping pressure was 0.08 MPa.32
In situ hybridization was used to detect mRNAs encoding EpCAM, CK8/18/19 (as epithelial biomarkers), or Vimentin and Twist (as mesenchymal biomarkers). The assay was performed in a 24-well plate (Corning, NY, USA), and the cells on the membrane were treated with a protease (Qiagen, Hilden, Germany) before hybridization with probe as previously described.11,31,33
CK19 Immunostaining and Scoring
Immunohistochemistry of HCC tissue samples after surgery was performed as previously described.34 Postoperative specimens were fixed in 10% formalin, embedded in paraffin, cut into 4-μm sections, deparaffinized in xylene and rehydrated through graded alcohol solutions. Antigen retrieval was performed for 2–3 min at 100°C in 10 mmol/L citrate buffer (pH 6.0) in a microwave oven. Endogenous peroxidases were blocked by immersing the sections in 3% hydrogen peroxide for 15 min. Sections were then incubated at 37°C for 1 hour with mouse antibody against CK19 (diluted 1:200; Kit-0030, Maixin, Fuzhou, China). Tissue sections were rinsed with PBS, incubated with anti-rabbit or -mouse immunoglobulin (Kit-5030; Maixin) diluted in PBS for 20 min at 25°C, and rinsed again with PBS. Finally, the samples were incubated with horseradish peroxidase-conjugated antibody for 10 min, rinsed in PBS, incubated with diaminobenzidine for 10 min, and counterstained with hematoxylin. CK19-positive tissue slices supplied with the immunostaining kits were analyzed in parallel with patient samples as positive controls and negative controls (by replacing primary antibody with PBS).
The proportion of all cells in the field of view of a section that stained for CK19 was determined independently by two senior pathologists who were blinded to clinical and follow-up data. When the proportion was >5%, the section was considered CK19-positive. Proportions of 5–10% were considered weak expression, while proportions >10% were considered strong expression.
The 105 patients were followed up every 1–2 months for the first year and every 3 months thereafter, with a final follow-up date of September 30, 2019. Postoperative follow-up consisted of one or more of the following tests: serum AFP measurement, ultrasonography, dynamic computed tomography (CT), and magnetic resonance imaging (MRI). Recurrence was diagnosed based on elevated AFP levels and findings on at least one of the three imaging modalities.35
All statistical analyses were performed with SPSS version 25 for Windows (IBM, Armonk, NY, USA). Scatter plots were plotted using GraphPrism Version 5.0 (GraphPad Software, La Jolla, CA, USA).
The rates of individuals with a given clinical or pathological characteristic, including a certain CTC count, were reported as n (%). Differences between groups were assessed for significance using the Pearson chi-squared test or Fisher’s exact tests if any cell number less than 5. Differences between patients with other CTC levels were assessed using the Mann–Whitney U-test because the data were not normally distributed.
A Kaplan–Meier curve with a Log rank test was performed to compare the tumor-free-survival (TFS) time between levels of CK19 expression or other groups. All statistical assessments were two-tailed, and differences associated with p < 0.05 were considered statistically significant.
Patient Characteristics and Clinical Outcomes
A total of 105 HCC patients with R0 resection (91 males and 14 females) with a mean age of 46.2 years (range: 20–72 years) were enrolled. Nearly half (43, 41.0%) were younger than 45 years, 75 (71.4%) had HBV-DNA levels ≥5.0×102, 59 (56.2%) had AFP levels ≥400 ng/mL, 40 (38.1%) presented multiple tumors, 48 (45.7%) were in BCLC stages B-C and 41 (39.0%) were incomplete tumor capsule. The demographic and clinical characteristics of the enrolled patients are summarized in Table 1.
Table 1 Demographic and Clinical Characteristics of the 105 HCC Patients
CK19 Immunostaining Levels and TFS
CK19 expression was detected in 27 of 105 (25.7%) HCC cases (Table 2, Figure 2A). TFS analyses showed that CK19-positive HCC patients had significantly shorter TFS than patients with CK19-negative tumors (median TFS:5 vs 10 months, P = 0.047) (Figure 2B). We also found that the characteristics of age<45, AFP≥400 ng/mL, and incomplete tumor capsule were more frequent among CK19-positive patients than CK19-negative ones (Table 2, Figure 2C–E). However, CK19 expression did not vary significantly with patient sex, HBsAg level, HBV-DNA level, tumor size, number of tumors, liver cirrhosis, Edmondson grade, BCLC stage, microvascular invasion (MVI) or portal vein tumor thrombus (PVTT) (Table 2).
Table 2 Comparison of Clinicopathological Characteristics Between HCC Patients Positive or Negative for CK19
CTC Subpopulations in Blood and Relationships to Clinical Characteristics
Using the CanPatrol™ CTC-enrichment technique, we measured the number of CTCs in the blood samples of 105 HCC patients before surgery. The green and red fluorescent signals represent mesenchymal or epithelial gene expression, respectively. Three subpopulations were identified: E-CTCs (Figure 3A), E/M-CTCs (Figure 3B), and M-CTCs (Figure 3C).
CTCs were detected in 98 (93.33%) of the 105 HCC patients. The preoperative median CTC count was 6 (range, 0–76). The 105 patients were divided into two sub-groups based on median CTC count: 48 (45.7%) patients were classified as having low total CTC count (<6) and 57 (54.3%) as having high CTC count (≥6) (Table 3).
Table 3 Comparison of Clinicopathological Characteristics Between HCC Patients with Low (<6) or High (≥6) CTC Counts
Significantly higher CTC counts were found in patients with AFP≥ 400 ng/mL, multiple tumors, HBV DNA≥5.0×102 and advanced HCC (BCLC B-C stage) (Table 3, Figure 3D–G). However, CTC counts did not vary significantly with patient age, sex, HBsAg level, tumor size, liver cirrhosis, Edmondson grade, tumor capsule, MVI or PVTT.
Association of CK19 Levels with CTC Count or Type
CK19-positive patients with high CTC count showed significantly higher CTC percentage (77.8%) than CK19-negative patients (46.2%, P = 0.004) (Figure 4A). Further analysis revealed that CTCs in peripheral blood of CK19-positive patients were mainly of the M-CTC type, whereas more CTCs were of the E-CTC type in CK19-negative patients (Table 4).
Table 4 Distribution of CTCs’ Types in 105 HCC Patients Positive or Negative for CK19
Our analysis found that the median TFS of the different groups were 5.0 months for CK19-positive patients with high CTC count, 7.0 months for CK19-negative patients with high CTC count, 7.0 months for CK19-positive patients with low CTC count, and 16.0 months for CK-negative patients with low CTC count. Among the four groups, patients who had high CTC count and were CK19-positive had significantly lower TFS (p<0.05) (Figure 4B).
The high recurrence and metastasis rates of HCC after radical surgery reduce survival. Therefore, early diagnosis of HCC and post-treatment monitoring are key for comprehensive treatment and management of these patients. At present, clinical indicators to predict postoperative recurrence are rare. Therefore, we explored the postoperative prognosis of HCC through the evaluation of preoperative peripheral blood CTCs levels as well as CK19 expression in postoperative cancer tissues.
CK19-positive HCC cells show a high degree of malignancy, including invasion and other aggressive behaviors.26,36–38 A previous study showed that the median disease-free survival time of CK19-positive HCC patients was significantly shorter than that of CK19-negative patients among those undergoing radiofrequency ablation.39 Consistently, we found that TFS was shorter for CK19-positive patients than for CK19-negative ones. Hepatocellular carcinoma recurrence is divided into early recurrence (less than 2 years) and late recurrence (more than 2 years) according to the time to recurrence after surgery.40–42 The mechanisms of early and late recurrence are different.43–46 The presence of CTCs reflects the aggressiveness of a solid tumor. A previous study by our group showed that high CTC counts before resection were significantly associated with early recurrence of HCC.31 The current work showed that CK19-positive patients had higher CTC counts than CK19-negative ones. We extended those findings in the present study by showing that high CTC count and CK19 express positive showed significantly lower tumor-free survival than patients with low CTC count and CK19-negative. These results suggest that CK19 contributes to poor prognosis.
We also found that CTCs in peripheral blood of CK19-positive patients were mainly of the M-CTC type, whereas more CTCs were of the E-CTC type in CK19-negative patients. M-CTCs are regarded as the most malignant CTC.31 A previous study revealed that CK19-positive cells in HCC possess Cancer stem cells (CSCs) characteristics are closely related to the EMT, and that CK19-positive cells express several genes associated with the EMT and show higher motility and migration than CK19-negative cells.26 EMT enhances tumor mobility and invasiveness and is believed to facilitate metastasis.47–49 During EMT, cancer cells lose some of their epithelial characteristics and acquire more migratory mesenchymal cell-like characteristics, undergoing major changes in their cytoskeleton.50,51 Our results suggest that high levels of M-CTCs are closely related to the expression of CK19 and lead to a poor prognosis in patients with CK19-positive HCC. CK19 may regulate EMT and promote an increase in the number of CTCs, ultimately leading to poor prognosis.
Interestingly, we found from the postoperative clinical results of HCC patients that those with CK19-positive HCC were younger, had higher serum AFP levels and showed lower rates of tumor envelope formation than those with CK19-negative HCC. These results suggest that the expression of CK19 in HCC increases tumor invasiveness.
This study presents several limitations. First, our cohort was relatively small. To overcome this limitation, we will further verify this conclusion in follow-up research and will conduct research in a multi-center cohort. In addition, the present study was conducted only at the clinical level. Molecular studies are needed to elucidate the causes of poor prognosis in CK19-positive patients with high CTCs in peripheral blood. This may help to find a new target for “precise therapy” for CK19-positive HCC patients with high preoperative CTC counts.
High CTC count and high M-CTC percentage are closely related to the expression of CK19 in HCC, which in turn is associated with recurrence. The preoperative number of CTCs undergoing EMT may be significantly higher in CK19-positive HCC patients than in CK19-negative patients. In CK-19 positive patients, the main CTC type may be mesenchymal. Preoperative CTC analysis combined with postoperative analysis of CK19 expression may be a new method for predicting prognosis of HCC patients after surgery.
This work was supported by grants from the National Natural Science Foundation of China (81960450), National Major Special Science and Technology Project (2017ZX10203207), The Key Research and Development Project of Guangxi (AA18221001, AB18050020), High-level innovation team and outstanding scholar program in Guangxi Colleges and Universities,“139” projects for training of high-level medical science talents from Guangxi(G201903001). The funding agencies had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
The authors report no conflicts of interest in this work.
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