Peritumoral ductular reaction: a poor postoperative prognostic factor for hepatocellular carcinoma

Hepatocellular carcinoma (HCC) is the fifth most common cancer worldwide [1]. Despite the great advancement in diagnosis and treatment modalities, especially surgical and targeted therapies, it’s outcome remains challenging due to frequent recurrence [2]. It is short of effective specific treatment after postoperative metastasis and recurrence in HCC [3]. Therefore, it is of great importance to seek optimal biomarkers that help predict early recurrence or metastasis.

HCC with progenitor cell features, possibly reflecting a progenitor cell origin, has a very bad prognosis [4]. Hepatic progenitor cells (HPCs) exhibit large nuclear-cytoplasmic ratio and oval-shaped nucleus, known as oval cells in rodents [5]. It is believed that HPCs are the descendants of stem cells. HPCs are scarce in the healthy liver, but upon stimulation, cells resident in the Canals of Hering proliferate across the hepatic lobule infiltrating the liver parenchyma [6]. HPCs can be observed by immunohistochemistry and electron microscope. The neoplastic cells are offspring of HPCs and each can differentiate a little differently, according to the local microenvironment in each part of the tumor if it explains the enormous phenotypic heterogeneity of a neoplasm [4]. In immunohistochemistry the phenotypes of HPCs express as OV6, CK7, CK19, CD133 and EPCAM [7‐9]. HPCs are verified to be able to differentiate into both hepatocytes and cholangiocytes when the latter fails to respond after severe injury [10].

HPCs form ductular reaction (DR), emanating from the portal zone and expanding into the parenchyma when they are activated to proliferate/differentiate, hepatocytic differentiation of these cells leads to the formation of intermediate hepatocytes [5]. Three types of DR are classically recognized, type 1, proliferation of pre-existing ducts and ductules; type 2, ductular metaplasia of hepatocytes and type 3, activation/proliferation of HPCs [11]. DR can be marked by immunostained with CK7 and CK19 [12, 13]. DR plays an important role in hepatocellular or cholangiocellular proliferation after virus related inflammation and damage. DR may represent a protective mechanism that allows intrahepatic cycling of bile acids to occur in chronic ductopenic biliary diseases [13]. Its immunostaining may help to identify small foci of invasion and to distinguish noninvasive, high-grade dysplastic nodules from both minimally invasive and overtly invasive HCC [12].

Activated and proliferative mechanism of HPCs is not clear, and inflammatory cytokine is considered as a key role in animal experiment [14]. Severity and location of inflammatory infiltration associated with activity and location of HPCs in chronic virus hepatitis [15]. Inflammation has emerged as the seventh hallmark of cancer [16]. Such prolonged self-replication in an inflammatory microenvironment could result in the accumulation of genetic lesions that cause cancer formation [17]. There is substantial evidence that the proinflammatory response at the tumor stroma could be rerouted into a tumor-promoting direction by stimulating angiogenesis and tissue remodeling [18].

However, the role of peritumoral DR in a necroinflammatory microenvironment remains to be elucidated in HCC. At the present study, we investigated DR and necroinflammatory microenvironment of patients with HCC. We also tried to uncover possible effect by correlating DR in a necroinflammatory microenvironment with postoperative prognosis in HCC.

To the best of our knowledge, this is the first study to identify peritumoral DR as an independent prognostic factor for HCC after resection. Patients with decreased peritumoral DR had a significantly prolonged OS and RFS compared with the increased subgroup. Therefore, patients with high peritumoral DR require closer follow-up after surgery, and peritumoral DR could also serve as a new biomarker predicting HCC recurrence.

DR occurs in cholestatic diseases, in inflammatory diseases and in conditions with massive loss of parenchyma [22‐24]. Hence, three types of DR are classically recognized [11]. We precluded the DR which originated from bile ducts obstructive diseases or cholestatic parenchymal damage in 106 patients with HCC, so the DR we observed could represent an activation of HPCs. Intermediate hepatobiliary cells of several differentiation states are continuously being produced in a dynamic nature of DR [25]. These data are supported by our results (Figures 2 and 3). DR is thought to arise due to a complex interaction between hepatocytes, hepatic progenitor cells, hepatic stellate cells and extracellular matrix as well as inflammatory cells and endothelial cells [13]. The total necroinflammatory score was significantly associated with the expansion of DR (Table 1). The result is in agreement with recent findings [26]. There was a highly significant correlation between the area of DR and fibrotic stage [27]. It may be important in the development of fibrosis [28]. These data are supported by our result showing that DR was significantly correlated with fibrotic stage (Table 1). Insulin resistance and hepatic inflammation might cause liver fibrosis by the expansion of the DR and the occurrence of epithelial-mesenchymal transition (EMT) [27‐29]. Our data showed that HPCs were in or closed to DR (Figures 2 and 3). Other authors proposed that DR is an important source of progenitor cells that can repopulate both the bile ductular and hepatocytic lineages in diseased liver [5, 30].

HPCs expansion forms DR by provided “field-effects” of a continuing necroinflammatory microenvironment. They were evidenced by their location in close proximity to the DR, and the strong correlation between these two variables [27]. The combination of interferon-γ and tumor necrosis factor alpha, cytokines overexpressed in HCV (Hepatitis C virus) may inhibit primary hepatocyte replication and stimulate HPCs expansion [31‐33]. Cellular signalling between HPCs and the surrounding nonparenchymal population is an important determinant of HPCs behaviour [34]. Our subsequent result showed that DR was higher in HBsAg (+) subgroup than in HBsAg (−), which meant that HPCs in DR expanded actively in HBsAg (+) (Table 2). ECM remodelling, such as fibrosis resolution and laminin deposition is likely to be important prerequisite to HPCs activation and expansion [35]. The collected evidence indicates that HPCs, in a suitable environment, could be induced to a direction of portal fibroblastic differentiation through EMT [36]. Chronic carbon tetrachloride (CCl₄) administration to mice induces significant hepatic fibrosis and can induce a florid HPCs response in parallel with advanced fibrosis [37]. It was suggested that the HPC response may drive liver fibrogenesis rather than being a secondary event [38].

Inflammation can supply bioactive molecules to the tumor microenvironment, including limiting cancer cell death [39, 40]. Necrotic cell death releases proinflammatory signals into the surrounding tissue microenvironment. As a consequence, necrotic cells can recruit inflammatory cells of the immune system [39, 41]. Additionally, necrotic cells can release bioactive regulatory factors, such as IL-1a, which can directly stimulate neighboring viable cells to proliferate [39]. Incipient neoplasias and potentially invasive and metastatic tumors may gain an advantage by tolerating some degree of necrotic cell death, doing so in order to recruit tumor-promoting inflammatory cells that bring growth-stimulating factors to the surviving cells within these growths [42].

DR expressing CK perhaps contains ones deriving from malignant degeneration of HPCs. The CK-positive HCC cells play the leading role in directing aggressive behavior of the tumor cell population [43]. The presence of CK19 expression by >5% of cells in HCC is associated with a poor prognosis [8]. The study of CK expression in the liver provides a useful insight into the mechanisms underlying progenitor cell activity and tissue regeneration following liver damage. HPCs express CK7 and CK19 [44]. They potentially derive from malignant degeneration of HPCs. HCC expressing CK19 had a higher incidence of AFP expression [8]. Our data showed that increased CK19-immunoreactive DR correlated with elevated serum AFP (Table 2). The higher recurrence rate of CK19 (+) HCC after transplantation suggests a worse prognosis for HCC expressing CK19 as compared to CK19 (−) HCC [8].

There are two types of recurrence for HCC: one is early recurrence, the other is late recurrence [21]. Discriminating between these two types is necessary in order to determine the appropriate intervention after surgery. True metastasis would benefit from adjuvant chemotherapy, while de novo cancer would be prevented by better control of viral infection and/or cirrhosis [45]. Our data showed that patients with early recurrence had significantly higher DR compared with patients with late recurrence. Patients with recurrence had especially higher DR and high necroinflammation compared with patients without recurrence, indicating the importance of alleviating necroinflammation, protecting hepatic function and strengthening general immunity. DR correlates with the degree of inflammation and fibrosis in the course of many chronic human liver diseases. Inflammation can supply bioactive molecules to the tumor microenvironment that facilitates inductive signals that lead to activation of EMT [39]. Some results indicated the critical association between the metastasis and EMT [46]. Mesenchymal stem cells in inflammation microenvironment accelerate HCC Metastasis by Inducing EMT [47]. DR may undergo the process of EMT in patients with the highest grade of necroinflammation [26]. Maybe the higher peritumoral DR was the prognostic indicator for early recurrence after hepatectomy due to intrahepatic metastasis through EMT.

The lack of liver donation, highly cost of operation and post-operative treatment, caused that few liver transplantation was carried out in our hospital. OS rates after hepatectomy for HCC was low. 5-yr survival after hepatectomy for HCC was 32.1% in this series. Because there were 71 (67%) patients with HCC whose tumor size was more than 5 cm, and the tumor size was independent prognostic factors for RFS and OS in our study. On the other hand, 67 (63.2%) patients had B/C of BCLC stage, 71 (67%) patients had II/III of TNM stage. Our study showed that increased peritumoral DR often correlated with multiple nodules and the absence of a tumor capsule, which are two features of a highly invasive HCC phenotype. Our study also showed that increased peritumoral DR correlated with severe microscopic vascular invasion. The cases with peritumoral multiple portal vein invasions tend to show early recurrence after hepatic resection. That’s the reason why it is common in early recurrence. Therefore, a very close follow-up protocol is required for patients with increased DR because it usually reveals highly aggressive tumor behavior.

In conclusion, we demonstrated for the first time that peritumoral DR in a necroinflammatory microenvironment is a poor prognostic factor for HCC following Resection. A continuing necroinflammatory microenvironment provides “field-effects” for stimulating HPCs expansion to form DR and partly to be diverted to malignant direction. DR expressing CK19 perhaps contains ones deriving from malignant degeneration of HPCs. Maybe the pretumoral DR is the prognostic indicator for early recurrence after hepatectomy due to intrahepatic metastasis through EMT. This provides a rationale for anti-inflammatory, anti-EMT and HPCs targeted therapies in clinical practice. Further experiments are needed to reveal the mechanisms of DR, EMT and inflammatory cells.