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The tumor microenvironment of VETC+ hepatocellular carcinoma is enriched of immunosuppressive TAMs spatially close to endothelial cells.
De Carlo, Camilla; Rosman-Nathanson, Roy; Durante, Barbara; Akpinar, Reha; Soldani, Cristiana; Franceschini, Barbara; Lasagni, Simone; Viganò, Luca; Procopio, Fabio; Costa, Guido; Torzilli, Guido; Lleo, Ana; Terracciano, Luigi Maria; Villa, Erica; Rimassa, Lorenza; Di Tommaso, Luca.
Affiliation
  • De Carlo C; Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Italy; Department of Pathology, IRCCS Humanitas Research Hospital, Rozzano, Italy.
  • Rosman-Nathanson R; Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Italy.
  • Durante B; Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Italy; Department of Pathology, IRCCS Humanitas Research Hospital, Rozzano, Italy.
  • Akpinar R; Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Italy.
  • Soldani C; Laboratory of Hepatobiliary Immunopathology, IRCCS Humanitas Research Hospital, Rozzano, Italy.
  • Franceschini B; Laboratory of Hepatobiliary Immunopathology, IRCCS Humanitas Research Hospital, Rozzano, Italy.
  • Lasagni S; Chimomo Department, Gastroenterology Unit, University of Modena and Reggio Emilia, Modena, Italy.
  • Viganò L; Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Italy; Hepatobiliary Unit, Department of Minimally Invasive General & Oncologic Surgery, Humanitas Gavazzeni University Hospital, Bergamo, Italy.
  • Procopio F; Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Italy; Division of Hepatobiliary and General Surgery, Department of Surgery, IRCCS Humanitas Research Hospital, Rozzano, Italy.
  • Costa G; Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Italy; Division of Hepatobiliary and General Surgery, Department of Surgery, IRCCS Humanitas Research Hospital, Rozzano, Italy.
  • Torzilli G; Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Italy; Division of Hepatobiliary and General Surgery, Department of Surgery, IRCCS Humanitas Research Hospital, Rozzano, Italy.
  • Lleo A; Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Italy; Division of Internal Medicine and Hepatology, Department of Gastroenterology, IRCCS Humanitas Research Hospital, Rozzano, Italy.
  • Terracciano LM; Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Italy; Department of Pathology, IRCCS Humanitas Research Hospital, Rozzano, Italy.
  • Villa E; Chimomo Department, Gastroenterology Unit, University of Modena and Reggio Emilia, Modena, Italy; UC Gastroenterologia, Dipartimento di Specialità Mediche, Azienda Ospedaliera Universitaria di Modena, Modena, Italy.
  • Rimassa L; Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Italy; Medical Oncology and Hematology Unit, Humanitas Cancer Center, IRCCS Humanitas Research Hospital, Rozzano, Italy.
  • Di Tommaso L; Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Italy; Department of Pathology, IRCCS Humanitas Research Hospital, Rozzano, Italy. Electronic address: luca.di_tommaso@hunimed.eu.
Dig Liver Dis ; 2024 Jun 29.
Article in En | MEDLINE | ID: mdl-38945759
ABSTRACT
BACKGROUND AND

AIM:

VETC (vessel that encapsulate tumor cluster) is a peculiar vascular phenotype observed in hepatocellular carcinoma (HCC), associated with distant metastases and poor outcome. VETC has been linked to the Tie2/Ang2 axis and is characterized by lymphocytes poor (cold) tumor microenvironment (TME). In this setting the role of Tumor Associated Macrophages (TAMs) has never been explored. Aim of the study is to investigate the presence and features of TAMs in VETC+ HCC and the possible interplay between TAMs and endothelial cells (ECs).

METHODS:

The series under study included 42 HCC. Once separated according to the VETC phenotype (21 VETC+; 21 VETC-) we stained consecutive slides with immunohistochemistry for CD68, CD163 and Tie2. Slides were then scanned and QuPath used to quantify morphological features.

RESULTS:

VETC+ cases were significantly (p < 0.001) enriched with large, lipid rich CD163+ TAMs (M2 oriented) that were spatially close to ECs; HCC cells significantly (p 0.002) overexpressed Tie2 with a polarization toward ECs.

CONCLUSIONS:

The pro-metastatic attitude of VETC is sustained by a strict morphological relationship between immunosuppressive M2-TAMs, ECs and Tie2-expressing HCC cells.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Dig Liver Dis Journal subject: GASTROENTEROLOGIA Year: 2024 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Dig Liver Dis Journal subject: GASTROENTEROLOGIA Year: 2024 Document type: Article Affiliation country: Country of publication: