NUCKS1 promotes invasion and metastasis of colorectal cancer by stabilizing HDAC2 and activating AKT

Abstract Nuclear ubiquitous casein and cyclin-dependent kinase substrate 1 (NUCKS1) functions as an oncogene in colorectal cancer (CRC), promotes the progression of CRC, and is associated with poor prognosis in patients. Studies have found that NUCKS1 promotes tumor cell metastasis, yet its role in...

Full description

Saved in:
Bibliographic Details
Main Authors: Liaoliao Zhu, Ting Zhao, Haichuan Su, Junqiang Li, Xiangjing Shen, Liang Zhang, Jun Chen, Yang Song
Format: Article
Language:English
Published: Nature Publishing Group 2025-06-01
Series:Oncogenesis
Online Access:https://doi.org/10.1038/s41389-025-00562-5
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1849685877936095232
author Liaoliao Zhu
Ting Zhao
Haichuan Su
Junqiang Li
Xiangjing Shen
Liang Zhang
Jun Chen
Yang Song
author_facet Liaoliao Zhu
Ting Zhao
Haichuan Su
Junqiang Li
Xiangjing Shen
Liang Zhang
Jun Chen
Yang Song
author_sort Liaoliao Zhu
collection DOAJ
description Abstract Nuclear ubiquitous casein and cyclin-dependent kinase substrate 1 (NUCKS1) functions as an oncogene in colorectal cancer (CRC), promotes the progression of CRC, and is associated with poor prognosis in patients. Studies have found that NUCKS1 promotes tumor cell metastasis, yet its role in CRC invasion and metastasis remains unclear. Our findings revealed higher NUCKS1 expression in metastatic CRC compared to non-metastatic samples. Upregulation of NUCKS1 expression promoted the migration and invasion of CRC cells, while knockdown of NUCKS1 significantly inhibited the migration and invasion of CRC cells. Mechanistically, NUCKS1 was initially found to upregulate HDAC2 expression by inhibiting the lysosomal pathway, activating AKT, and thus promoting CRC invasion and metastasis. Moreover, HDAC2 inhibitor Santacruzamate A or AKT inhibitor LY294002 rescued the migration and invasion of CRC cells caused by NUCKS1 overexpression. In vivo, by injecting CRC cells into the tail vein of a nude mouse model, we found that overexpression of NUCKS1-induced lung and liver metastasis was suppressed by HDAC2 knockdown or intraperitoneal administration of the HDAC2 inhibitor Santacruzamate A. Meanwhile, AKT inhibitor LY294002 significantly inhibited lung and liver metastasis caused by overexpression of HDAC2. The expression levels of NUCKS1, HDAC2, and phosphorylated AKT were significantly positively correlated in human CRC tissues. These findings suggest that NUCKS1 contributes to CRC invasion and metastasis by stabilizing HDAC2 and activating AKT, highlighting NUCKS1 and HDAC2 as potential therapeutic targets for CRC.
format Article
id doaj-art-98f039bfcc434bafabe18bdc4a942599
institution DOAJ
issn 2157-9024
language English
publishDate 2025-06-01
publisher Nature Publishing Group
record_format Article
series Oncogenesis
spelling doaj-art-98f039bfcc434bafabe18bdc4a9425992025-08-20T03:22:55ZengNature Publishing GroupOncogenesis2157-90242025-06-0114111210.1038/s41389-025-00562-5NUCKS1 promotes invasion and metastasis of colorectal cancer by stabilizing HDAC2 and activating AKTLiaoliao Zhu0Ting Zhao1Haichuan Su2Junqiang Li3Xiangjing Shen4Liang Zhang5Jun Chen6Yang Song7Department of Oncology, Tangdu Hospital, Air Force Medical UniversityDepartment of Oncology, Tangdu Hospital, Air Force Medical UniversityDepartment of Oncology, Tangdu Hospital, Air Force Medical UniversityDepartment of Oncology, Tangdu Hospital, Air Force Medical UniversityDepartment of Oncology, Tangdu Hospital, Air Force Medical UniversityDepartment of Oncology, Tangdu Hospital, Air Force Medical UniversityOrthopedics Department of Xi’an People’s Hospital (Xi’an Fourth Hospital)Department of Oncology, Tangdu Hospital, Air Force Medical UniversityAbstract Nuclear ubiquitous casein and cyclin-dependent kinase substrate 1 (NUCKS1) functions as an oncogene in colorectal cancer (CRC), promotes the progression of CRC, and is associated with poor prognosis in patients. Studies have found that NUCKS1 promotes tumor cell metastasis, yet its role in CRC invasion and metastasis remains unclear. Our findings revealed higher NUCKS1 expression in metastatic CRC compared to non-metastatic samples. Upregulation of NUCKS1 expression promoted the migration and invasion of CRC cells, while knockdown of NUCKS1 significantly inhibited the migration and invasion of CRC cells. Mechanistically, NUCKS1 was initially found to upregulate HDAC2 expression by inhibiting the lysosomal pathway, activating AKT, and thus promoting CRC invasion and metastasis. Moreover, HDAC2 inhibitor Santacruzamate A or AKT inhibitor LY294002 rescued the migration and invasion of CRC cells caused by NUCKS1 overexpression. In vivo, by injecting CRC cells into the tail vein of a nude mouse model, we found that overexpression of NUCKS1-induced lung and liver metastasis was suppressed by HDAC2 knockdown or intraperitoneal administration of the HDAC2 inhibitor Santacruzamate A. Meanwhile, AKT inhibitor LY294002 significantly inhibited lung and liver metastasis caused by overexpression of HDAC2. The expression levels of NUCKS1, HDAC2, and phosphorylated AKT were significantly positively correlated in human CRC tissues. These findings suggest that NUCKS1 contributes to CRC invasion and metastasis by stabilizing HDAC2 and activating AKT, highlighting NUCKS1 and HDAC2 as potential therapeutic targets for CRC.https://doi.org/10.1038/s41389-025-00562-5
spellingShingle Liaoliao Zhu
Ting Zhao
Haichuan Su
Junqiang Li
Xiangjing Shen
Liang Zhang
Jun Chen
Yang Song
NUCKS1 promotes invasion and metastasis of colorectal cancer by stabilizing HDAC2 and activating AKT
Oncogenesis
title NUCKS1 promotes invasion and metastasis of colorectal cancer by stabilizing HDAC2 and activating AKT
title_full NUCKS1 promotes invasion and metastasis of colorectal cancer by stabilizing HDAC2 and activating AKT
title_fullStr NUCKS1 promotes invasion and metastasis of colorectal cancer by stabilizing HDAC2 and activating AKT
title_full_unstemmed NUCKS1 promotes invasion and metastasis of colorectal cancer by stabilizing HDAC2 and activating AKT
title_short NUCKS1 promotes invasion and metastasis of colorectal cancer by stabilizing HDAC2 and activating AKT
title_sort nucks1 promotes invasion and metastasis of colorectal cancer by stabilizing hdac2 and activating akt
url https://doi.org/10.1038/s41389-025-00562-5
work_keys_str_mv AT liaoliaozhu nucks1promotesinvasionandmetastasisofcolorectalcancerbystabilizinghdac2andactivatingakt
AT tingzhao nucks1promotesinvasionandmetastasisofcolorectalcancerbystabilizinghdac2andactivatingakt
AT haichuansu nucks1promotesinvasionandmetastasisofcolorectalcancerbystabilizinghdac2andactivatingakt
AT junqiangli nucks1promotesinvasionandmetastasisofcolorectalcancerbystabilizinghdac2andactivatingakt
AT xiangjingshen nucks1promotesinvasionandmetastasisofcolorectalcancerbystabilizinghdac2andactivatingakt
AT liangzhang nucks1promotesinvasionandmetastasisofcolorectalcancerbystabilizinghdac2andactivatingakt
AT junchen nucks1promotesinvasionandmetastasisofcolorectalcancerbystabilizinghdac2andactivatingakt
AT yangsong nucks1promotesinvasionandmetastasisofcolorectalcancerbystabilizinghdac2andactivatingakt