Abstract
Background
Twenty percent of children with hepatoblastoma (HB) have lung metastasis at diagnosis. Treatment protocols recommend surgical removal of chemotherapy-refractory lung nodules, however no chronological order is established. As hepatectomy is followed by release of growth factors, it has been proposed that partial hepatectomy (PH) could boost local or distant residual tumor growth.
Methods
To evaluate the impact of PH on distant tumor growth, PH was performed in mice subcutaneously implanted with a HB patient-derived xenograft (PDX). The influence of PH on tumor growth at primary site was assessed by performing PH concomitantly to HB PDXs orthotopic implantation.
Results
Subcutaneously implanted HB PDX failed to show any influence of hepatectomy on tumor growth. Instead, intrahepatic tumor growth of one of the 4 HB PDXs implanted orthotopically was clearly enhanced. Cells derived from the hepatectomy-sensitive HB PDX exposed to hepatic growth factor (HGF) showed increased proliferation rate compared to cells derived from a hepatectomy-insensitive model, suggesting that the HGF/MET pathway could be one of the effectors of the crosstalk between liver regeneration and HB growth.
Conclusion
These results suggest that hepatectomy can contribute to HB growth in some patients, further studies will be necessary to identify biomarkers predictive of patient risk of PH-induced HB recurrence.
Impact
-
Key message: Cytokines and growth factors secreted following partial hepatectomy can contribute to intrahepatic tumor growth in some hepatoblastoma models.
-
What does it add to the existing literature: It is the first article about the impact of liver regeneration induced by partial hepatectomy on hepatoblastoma local or distant tumoral growth in nude mice.
-
What is the impact: It is important to identify the secreted factors that enhance tumor growth and to define biomarkers predictive of patient risk of partial hepatectomy-induced hepatoblastoma recurrence.
This is a preview of subscription content, access via your institution
Access options
Subscribe to this journal
Receive 14 print issues and online access
$259.00 per year
only $18.50 per issue
Buy this article
- Purchase on SpringerLink
- Instant access to full article PDF
Prices may be subject to local taxes which are calculated during checkout
Similar content being viewed by others
Data availability
The datasets generated during and/or analyzed during the current study are available from the corresponding author on reasonable request.
References
Aronson, D. C., Czauderna, P., Maibach, R., Perilongo, G., Morland, B. The treatment of hepatoblastoma: its evolution and the current status as per the SIOPEL trials. J. Indian Assoc. Pediatr. Surg. 19, 201–207 (2014).
Spector, L. G. & Birch, J. The epidemiology of hepatoblastoma. Pediatr. Blood Cancer 59, 776–779 (2012).
Weinberg, A. G. & Finegold, M. J. Primary hepatic tumors of childhood. Hum. Pathol. 14, 512–537 (1983).
López-Terrada, D. et al. Towards an international pediatric liver tumor consensus classification: proceedings of the Los Angeles COG liver tumors symposium. Mod. Pathol. 27, 472–491 (2014).
Cairo, S. et al. Hepatic stem-like phenotype and interplay of Wnt/β-Catenin and Myc signaling in aggressive childhood liver cancer. Cancer Cell 14, 471–484 (2008).
Czauderna, P. et al. Hepatoblastoma state of the art: pathology, genetics, risk stratification, and chemotherapy. Curr. Opin. Pediatr. 26, 19–28 (2014).
Evans, A. E. et al. Combination chemotherapy (vincristine, adriamycin, cyclophosphamide, and 5-fluorouracil) in the treatment of children with malignant hepatoma. Cancer 50, 821–826 (1982).
Weinblatt, M. E., Siegel, S. E., Siegel, M. M., Stanley, P. & Weitzman, J. J. Preoperative chemotherapy for unresectable primary hepatic malignancies in children. Cancer 50, 1061–1064 (1982).
Ninane, J. et al. Effectiveness and toxicity of cisplatin and doxorubicin (PLADO) in childhood hepatoblastoma and hepatocellular carcinoma: a siop pilot study. Med. Pediatr. Oncol. 19, 199–203 (1991).
Ortega, J. A. et al. Effective treatment of unresectable or metastatic hepatoblastoma with cisplatin and continuous infusion doxorubicin chemotherapy: a report from the Childrens Cancer Study Group. J. Clin. Oncol. 9, 2167–2176 (1991).
Douglass, E. C., Reynolds, M., Finegold, M., Cantor, A. B. & Glicksman, A. Cisplatin, vincristine, and fluorouracil therapy for hepatoblastoma: a Pediatric Oncology Group study. J. Clin. Oncol. 11, 96–99 (1993).
Fuchs, J., Seitz, G., Handgretinger, R., Schäfer, J. & Warmann, S. W. Surgical treatment of lung metastases in patients with embryonal pediatric solid tumors: an update. Semin. Pediatr. Surg. 21, 79–87 (2012).
Häcker, F. M., Von Schweinitz, D. & Gambazzi, F. The relevance of surgical therapy for bilateral and/or multiple pulmonary metastases in children. Eur. J. Pediatr. Surg. 17, 84–89 (2007).
Meyers, R. L. et al. Surgical resection of pulmonary metastatic lesions in children with hepatoblastoma. J. Pediatr. Surg. 42, 2050–2056 (2007).
Urla, C. et al. Simultaneous resection of high-risk liver tumors and pulmonary metastases in children. Ann. Surg. 262, e1–e3 (2015).
Exelby, P. R., Filler, R. M. & Grosfeld, J. L. Liver tumors in children in the particular reference to hepatoblastoma and hepatocellular carcinoma: American academy of pediatrics surgical section survey — 1974. J. Pediatr. Surg. 10, 329–337 (1975).
Shamberger, R. C., Leichtner, A. M., Jonas, M. M. & LaQuaglia, M. P. Long-term hepatic regeneration and function in infants and children following liver resection. J. Am. Coll. Surg. 182, 515–519 (1996).
Lim, C. et al. Tumour progression and liver regeneration–insights from animal models. Nat. Rev. Gastroenterol. Hepatol. 10, 452–462 (2013).
Panis, Y., Ribeiro, J., Chrétien, Y. & Nordlinger, B. Dormant liver metastases: an experimental study. Br. J. Surg. 79, 221–223 (1992).
Slooter, G. D., Marquet, R. L., Jeekel, J. & Ijzermans, J. N. M. Tumour growth stimulation after partial hepatectomy can be reduced by treatment with tumour necrosis factor α. Br. J. Surg. 82, 129–132 (1995).
de Jong, K. P. et al. The effect of partial hepatectomy on tumor growth in rats: In vivo and in vitro studies. Hepatology 22, 1263–1272 (1995).
Rashidi, B. et al. Minimal liver resection strongly stimulates the growth of human colon cancer in the liver of nude mice. Clin. Exp. Metastasis 17, 497–500 (1999).
Harun, N., Nikfarjam, M., Muralidharan, V. & Christophi, C. Liver regeneration stimulates tumor metastases. J. Surg. Res. 138, 284–290 (2007).
Momiyama, M. et al. Major liver resection stimulates stromal recruitment and metastasis compared with repeated minor resection. J. Surg. Res. 178, 280–287 (2012).
von Schweinitz, D., Fuchs, J., Glüer, S. & Pietsch, T. The occurrence of liver growth factor in hepatoblastoma. Eur. J. Pediatr. Surg. 8, 133–136 (1998).
Shi, J. H. & Line, P. M. Effect of liver regeneration on malignant hepatic tumors. World J. Gastroenterol. 20, 16167–16177 (2014).
Nicolle, D. et al. Patient-derived mouse xenografts from pediatric liver cancer predict tumor recurrence and advise clinical management. Hepatology 64, 1121–1135 (2016).
Kats, D. et al. Volasertib preclinical activity in high-risk hepatoblastoma. Oncotarget 10, 6403–6417 (2019).
Eloranta, K. et al. Chloroquine triggers cell death and inhibits PARPs in cell models of aggressive hepatoblastoma. Front. Oncol. 10, 1138 (2020).
Michalopoulos, G. K. Liver regeneration. J. Cell Physiol. 213, 286–300 (2007).
von Schweinitz, D. et al. Hepatocyte growth factor- scatter factor can stimulate post-operative tumor-cell proliferation in childhood hepatoblastoma. Int. J. Cancer 85, 151–159 (2000).
Vidal, I. & Richert, L. The nude mouse as model for liver deficiency study and treatment and xenotransplantation. Int. J. Hepatol. 2012, 140147 (2012).
Paschkis, K. E., Cantarow, A., Stasney, J. & Hobbs, J. H. Tumor growth in partially hepatectomized rats. Cancer Res. 15, 579 (1955).
Schindel, D. T. & Grosfeld, J. L. Hepatic resection enhances growth of residual intrahepatic and subcutaneous hepatoma, which is inhibited by octreotide. J. Pediatr. Surg. 32, 995–997 (1997).
Gutman, M., Singh, R. K., Price, J. E., Fan, D. & Fidler, I. J. Accelerated growth of human colon cancer cells in nude mice undergoing liver regeneration. Invasion Metastasis 14, 362–371 (1994).
Schnater, J. M. et al. Subcutaneous and intrahepatic growth of human hepatoblastoma in immunodeficient mice. J. Hepatol. 45, 377–386 (2006).
Ellerkamp, V. et al. Successful establishment of an orthotopic hepatoblastoma in vivo model in NOD/LtSz-scid IL2Rγnull mice. PLoS One 6, e23419 (2011).
Chen, X. & Calvisi, D. F. Hydrodynamic transfection for generation of novel mouse models for liver cancer research. Am. J. Pathol. 184, 912–923 (2014).
Armengol, C. et al. Orthotopic implantation of human hepatocellular carcinoma in mice. Clin. Cancer Res. 10, 2150 (2004).
Bissig-Choisat, B. et al. Novel patient-derived xenograft and cell line models for therapeutic testing of pediatric liver cancer. J. Hepatol. 65, 325–333 (2016).
Acknowledgements
We are grateful to all the technicians from XenTech’s in vivo facility for their contribution in the study.
Funding
The study was supported and financed by XenTech; M.C. received a fellowship from SFCP (Societé Française de Chirurgie Pédiatrique).
Author information
Authors and Affiliations
Contributions
Conception and design: M.C., S.C. and S.B. Acquisition of data: M.C., L.B.S., V.B., C.M., C.G. Analysis and interpretation of data: M.C., L.B.S., O.D., C.M., C.G., M.F. Revising the article: T.T., M.P., J.G.J. Final approval of the version to be published: M.C., S.C. and S.B. All authors have read and agreed to the published version of the manuscript.”
Corresponding authors
Ethics declarations
Competing interests
The authors declare no competing interests.
Additional information
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary Information
Rights and permissions
Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.
About this article
Cite this article
Cornet, M., Brulle-Soumare, L., Bisio, V. et al. Modelling the impact of liver regeneration on hepatoblastoma patient-derived-xenograft tumor growth. Pediatr Res (2024). https://doi.org/10.1038/s41390-024-03020-x
Received:
Revised:
Accepted:
Published:
DOI: https://doi.org/10.1038/s41390-024-03020-x