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Novel High-Throughput Screen Identified S100A4 Inhibitors for Anti-Metastatic Therapy
by
Heisterkamp, Nina
, Schütz, Devin
, Putzker, Kerstin
, Uhrig, Ulrike
, Walther, Wolfgang
, Kobelt, Dennis
, Schöpe, Paul Curtis
, Mastrobuoni, Guido
, Nazaré, Marc
, Kempa, Stefan
, Stein, Ulrike
in
Animals
/ Antineoplastic Agents - pharmacology
/ Cell Line, Tumor
/ Cell Movement - drug effects
/ Cell Proliferation - drug effects
/ Colorectal Neoplasms - drug therapy
/ Colorectal Neoplasms - metabolism
/ Colorectal Neoplasms - pathology
/ HCT116 Cells
/ High-Throughput Screening Assays - methods
/ Humans
/ Mice
/ Mice, Nude
/ Neoplasm Metastasis
/ Research Paper
/ S100 Calcium-Binding Protein A4 - antagonists & inhibitors
/ S100 Calcium-Binding Protein A4 - metabolism
/ S100 Proteins - antagonists & inhibitors
/ S100 Proteins - genetics
/ S100 Proteins - metabolism
/ Xenograft Model Antitumor Assays
2025
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Novel High-Throughput Screen Identified S100A4 Inhibitors for Anti-Metastatic Therapy
by
Heisterkamp, Nina
, Schütz, Devin
, Putzker, Kerstin
, Uhrig, Ulrike
, Walther, Wolfgang
, Kobelt, Dennis
, Schöpe, Paul Curtis
, Mastrobuoni, Guido
, Nazaré, Marc
, Kempa, Stefan
, Stein, Ulrike
in
Animals
/ Antineoplastic Agents - pharmacology
/ Cell Line, Tumor
/ Cell Movement - drug effects
/ Cell Proliferation - drug effects
/ Colorectal Neoplasms - drug therapy
/ Colorectal Neoplasms - metabolism
/ Colorectal Neoplasms - pathology
/ HCT116 Cells
/ High-Throughput Screening Assays - methods
/ Humans
/ Mice
/ Mice, Nude
/ Neoplasm Metastasis
/ Research Paper
/ S100 Calcium-Binding Protein A4 - antagonists & inhibitors
/ S100 Calcium-Binding Protein A4 - metabolism
/ S100 Proteins - antagonists & inhibitors
/ S100 Proteins - genetics
/ S100 Proteins - metabolism
/ Xenograft Model Antitumor Assays
2025
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Novel High-Throughput Screen Identified S100A4 Inhibitors for Anti-Metastatic Therapy
by
Heisterkamp, Nina
, Schütz, Devin
, Putzker, Kerstin
, Uhrig, Ulrike
, Walther, Wolfgang
, Kobelt, Dennis
, Schöpe, Paul Curtis
, Mastrobuoni, Guido
, Nazaré, Marc
, Kempa, Stefan
, Stein, Ulrike
in
Animals
/ Antineoplastic Agents - pharmacology
/ Cell Line, Tumor
/ Cell Movement - drug effects
/ Cell Proliferation - drug effects
/ Colorectal Neoplasms - drug therapy
/ Colorectal Neoplasms - metabolism
/ Colorectal Neoplasms - pathology
/ HCT116 Cells
/ High-Throughput Screening Assays - methods
/ Humans
/ Mice
/ Mice, Nude
/ Neoplasm Metastasis
/ Research Paper
/ S100 Calcium-Binding Protein A4 - antagonists & inhibitors
/ S100 Calcium-Binding Protein A4 - metabolism
/ S100 Proteins - antagonists & inhibitors
/ S100 Proteins - genetics
/ S100 Proteins - metabolism
/ Xenograft Model Antitumor Assays
2025
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Novel High-Throughput Screen Identified S100A4 Inhibitors for Anti-Metastatic Therapy
Journal Article
Novel High-Throughput Screen Identified S100A4 Inhibitors for Anti-Metastatic Therapy
2025
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Overview
Colorectal cancer (CRC) metastasis continues to account for a substantial proportion of cancer-related deaths worldwide. Calcium-binding protein S100A4 is a known executor of CRC metastasis. S100A4 has been correlated to metastasis formation in the past, and therefore pharmaceutical intervention reduces the metastatic phenotype. Herein, a high-throughput screen (HTS) of 105,600 compounds from the EMBL screening library using an S100A4 promoter-driven luciferase construct transfected into HCT116 cells identified novel compounds for S100A4 transcriptional inhibition. The most promising inhibitors identified were tested for S100A4 transcriptional inhibition, their impact on wound healing, migration, proliferation and viability of cancer cells. Subsequently, the leading candidate E12 was tested
in a xenograft mouse model (HCT116/CMVp- Luc). After several testing rounds, E12 a 2-(4-fluorobenzenesulfonamido)benzamide-based compound showed the strongest inhibition of S100A4 expression at mRNA (EC
< 1 µM; 48 h) and protein level and concomitant restriction of metastatic abilities in two CRC cell lines with a tolerable viability reduction.
, a reduction in metastasis formation was demonstrated, displayed by reduced overall bioluminescence of tumors and human satellite DNA in the liver of treated mice. This study exhibited E12's promising potential for S100A4 targeted metastasis inhibition therapy to improve the outcome of metastasized CRC patients.
Publisher
Ivyspring International Publisher
Subject
/ Antineoplastic Agents - pharmacology
/ Cell Movement - drug effects
/ Cell Proliferation - drug effects
/ Colorectal Neoplasms - drug therapy
/ Colorectal Neoplasms - metabolism
/ Colorectal Neoplasms - pathology
/ High-Throughput Screening Assays - methods
/ Humans
/ Mice
/ S100 Calcium-Binding Protein A4 - antagonists & inhibitors
/ S100 Calcium-Binding Protein A4 - metabolism
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