Saved in:
Bibliographic Details
Main Authors: Rajbongshi, Lata, Kim, Ji-Eun, Lee, Jin-Eui, Lee, Su-Rin, Hwang, Seon-Yeong, Kim, Yuna, Hong, Young Mi, Oh, Sae-Ock, Kim, Byoung Soo, Lee, Dongjun, Yoon, Sik
Format: Artículo científico
Language:en
Published: Marine drugs 2025
Subjects:
Online Access:https://pubmed.ncbi.nlm.nih.gov/41149589/
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1868266136439619585
author Rajbongshi, Lata
Kim, Ji-Eun
Lee, Jin-Eui
Lee, Su-Rin
Hwang, Seon-Yeong
Kim, Yuna
Hong, Young Mi
Oh, Sae-Ock
Kim, Byoung Soo
Lee, Dongjun
Yoon, Sik
author_facet Rajbongshi, Lata
Kim, Ji-Eun
Lee, Jin-Eui
Lee, Su-Rin
Hwang, Seon-Yeong
Kim, Yuna
Hong, Young Mi
Oh, Sae-Ock
Kim, Byoung Soo
Lee, Dongjun
Yoon, Sik
Rajbongshi, Lata
Kim, Ji-Eun
Lee, Jin-Eui
Lee, Su-Rin
Hwang, Seon-Yeong
Kim, Yuna
Hong, Young Mi
Oh, Sae-Ock
Kim, Byoung Soo
Lee, Dongjun
Yoon, Sik
collection PubMed - marine biology
contents A Robust Marine Collagen Peptide-Agarose 3D Culture System for In Vitro Modeling of Hepatocellular Carcinoma and Anti-Cancer Therapeutic Development. Rajbongshi, Lata Kim, Ji-Eun Lee, Jin-Eui Lee, Su-Rin Hwang, Seon-Yeong Kim, Yuna Hong, Young Mi Oh, Sae-Ock Kim, Byoung Soo Lee, Dongjun Yoon, Sik Carcinoma, Hepatocellular Humans Liver Neoplasms Collagen Spheroids, Cellular Antineoplastic Agents Cell Line, Tumor Hydrogels Cell Proliferation Neoplastic Stem Cells Peptides Epithelial-Mesenchymal Transition Cell Culture Techniques, Three Dimensional Animals Aquatic Organisms The development of physiologically relevant three-dimensional (3D) culture systems is essential for modeling tumor complexity and improving the translational impact of cancer research. We established a 3D in vitro model of human hepatocellular carcinoma (HCC) using a marine collagen peptide-based (MCP-B) biomimetic hydrogel scaffold optimized for multicellular spheroid growth. Compared with conventional two-dimensional (2D) cultures, the MCP-B hydrogel more accurately recapitulated native tumor biology while offering simplicity, reproducibility, bioactivity, and cost efficiency. HCC cells cultured in MCP-B hydrogel displayed tumor-associated behaviors, including enhanced proliferation, colony formation, migration, invasion, and chemoresistance, and enriched cancer stem cell (CSC) populations. Molecular analyses revealed upregulated expression of genes associated with multidrug resistance; stemness regulation and markers; epithelial-mesenchymal transition (EMT) transcription factors, markers, and effectors; growth factors and their receptors; and cancer progression. The spheroids also retained liver-specific functions, suppressed apoptotic signaling, and exhibited extracellular matrix remodeling signatures. Collectively, these findings demonstrate that the 3D HCC model using MCP-B hydrogel recapitulates key hallmarks of tumor biology and provides a robust, physiologically relevant platform for mechanistic studies of HCC and CSC biology. This model further holds translational value for preclinical drug screening and the development of novel anti-HCC and anti-CSC therapeutics.
format Artículo científico
id pubmed_41149589
institution PubMed
language en
publishDate 2025
publisher Marine drugs
record_format pubmed
spellingShingle A Robust Marine Collagen Peptide-Agarose 3D Culture System for In Vitro Modeling of Hepatocellular Carcinoma and Anti-Cancer Therapeutic Development.
Rajbongshi, Lata
Kim, Ji-Eun
Lee, Jin-Eui
Lee, Su-Rin
Hwang, Seon-Yeong
Kim, Yuna
Hong, Young Mi
Oh, Sae-Ock
Kim, Byoung Soo
Lee, Dongjun
Yoon, Sik
Carcinoma, Hepatocellular
Humans
Liver Neoplasms
Collagen
Spheroids, Cellular
Antineoplastic Agents
Cell Line, Tumor
Hydrogels
Cell Proliferation
Neoplastic Stem Cells
Peptides
Epithelial-Mesenchymal Transition
Cell Culture Techniques, Three Dimensional
Animals
Aquatic Organisms
A Robust Marine Collagen Peptide-Agarose 3D Culture System for In Vitro Modeling of Hepatocellular Carcinoma and Anti-Cancer Therapeutic Development. Rajbongshi, Lata Kim, Ji-Eun Lee, Jin-Eui Lee, Su-Rin Hwang, Seon-Yeong Kim, Yuna Hong, Young Mi Oh, Sae-Ock Kim, Byoung Soo Lee, Dongjun Yoon, Sik Carcinoma, Hepatocellular Humans Liver Neoplasms Collagen Spheroids, Cellular Antineoplastic Agents Cell Line, Tumor Hydrogels Cell Proliferation Neoplastic Stem Cells Peptides Epithelial-Mesenchymal Transition Cell Culture Techniques, Three Dimensional Animals Aquatic Organisms The development of physiologically relevant three-dimensional (3D) culture systems is essential for modeling tumor complexity and improving the translational impact of cancer research. We established a 3D in vitro model of human hepatocellular carcinoma (HCC) using a marine collagen peptide-based (MCP-B) biomimetic hydrogel scaffold optimized for multicellular spheroid growth. Compared with conventional two-dimensional (2D) cultures, the MCP-B hydrogel more accurately recapitulated native tumor biology while offering simplicity, reproducibility, bioactivity, and cost efficiency. HCC cells cultured in MCP-B hydrogel displayed tumor-associated behaviors, including enhanced proliferation, colony formation, migration, invasion, and chemoresistance, and enriched cancer stem cell (CSC) populations. Molecular analyses revealed upregulated expression of genes associated with multidrug resistance; stemness regulation and markers; epithelial-mesenchymal transition (EMT) transcription factors, markers, and effectors; growth factors and their receptors; and cancer progression. The spheroids also retained liver-specific functions, suppressed apoptotic signaling, and exhibited extracellular matrix remodeling signatures. Collectively, these findings demonstrate that the 3D HCC model using MCP-B hydrogel recapitulates key hallmarks of tumor biology and provides a robust, physiologically relevant platform for mechanistic studies of HCC and CSC biology. This model further holds translational value for preclinical drug screening and the development of novel anti-HCC and anti-CSC therapeutics.
title A Robust Marine Collagen Peptide-Agarose 3D Culture System for In Vitro Modeling of Hepatocellular Carcinoma and Anti-Cancer Therapeutic Development.
topic Carcinoma, Hepatocellular
Humans
Liver Neoplasms
Collagen
Spheroids, Cellular
Antineoplastic Agents
Cell Line, Tumor
Hydrogels
Cell Proliferation
Neoplastic Stem Cells
Peptides
Epithelial-Mesenchymal Transition
Cell Culture Techniques, Three Dimensional
Animals
Aquatic Organisms
url https://pubmed.ncbi.nlm.nih.gov/41149589/