APOC1 knockdown induces apoptosis and decreases angiogenesis in diffuse large B-cell lymphoma cells through blocking the PI3K/AKT/mTOR pathway

Diffuse large B-cell lymphoma (DLBCL) is a highly heterogeneous metastatic lymphoma that can be treated by targeting angiogenesis. Apolipoprotein C1 (APOC1) plays a significant role in the proliferation and metastasis of various malignant tumors; however, its role in DLBCL—particularly its effects o...

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Main Authors: Jing Gao, Xiaojuan Lu, Guanglei Wang, Tanling Huang, Zhongyu Tuo, Weiwei Meng
Format: Article
Language:English
Published: Association of Basic Medical Sciences of Federation of Bosnia and Herzegovina 2025-01-01
Series:Biomolecules & Biomedicine
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Online Access:https://bjbms.org/ojs/index.php/bjbms/article/view/11550
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author Jing Gao
Xiaojuan Lu
Guanglei Wang
Tanling Huang
Zhongyu Tuo
Weiwei Meng
author_facet Jing Gao
Xiaojuan Lu
Guanglei Wang
Tanling Huang
Zhongyu Tuo
Weiwei Meng
author_sort Jing Gao
collection DOAJ
description Diffuse large B-cell lymphoma (DLBCL) is a highly heterogeneous metastatic lymphoma that can be treated by targeting angiogenesis. Apolipoprotein C1 (APOC1) plays a significant role in the proliferation and metastasis of various malignant tumors; however, its role in DLBCL—particularly its effects on angiogenesis—remains largely unexplored. This study investigates the correlation between APOC1 expression and patient prognosis in DLBCL. Using APOC1 gene knockdown, apoptosis, migration, and invasion were assessed through flow cytometry, the EDU assay, wound healing, and Transwell assays. Additionally, human umbilical vein endothelial cells (HUVEC) angiogenesis was evaluated. Advanced techniques, such as immunofluorescence, TUNEL assay, and immunohistochemical labeling were employed to analyze the effects of APOC1 knockdown on the PI3K/AKT/mTOR signaling pathway and tumor formation in nude mice. Results showed that APOC1 is overexpressed in DLBCL tissues and cells, with high APOC1 levels associated with poor patient prognosis. In vitro experiments revealed that APOC1 knockdown increased apoptosis and inhibited cell proliferation, migration, invasion, HUVEC angiogenesis, and PI3K/AKT/mTOR signaling pathway protein expression in DLBCL cells. Similarly, in vivo studies demonstrated that APOC1 knockdown significantly reduced tumor growth, angiogenesis-related proteins, and phosphorylated PI3K/AKT/mTOR pathway proteins in nude mice. APOC1 knockdown promotes apoptosis and suppresses angiogenesis in DLBCL cells by inhibiting the PI3K/AKT/mTOR pathway.
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institution Kabale University
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spelling doaj-art-0c305457f6ab4c3698ac1402ffdfc9b12025-02-03T16:42:10ZengAssociation of Basic Medical Sciences of Federation of Bosnia and HerzegovinaBiomolecules & Biomedicine2831-08962831-090X2025-01-0110.17305/bb.2024.11550APOC1 knockdown induces apoptosis and decreases angiogenesis in diffuse large B-cell lymphoma cells through blocking the PI3K/AKT/mTOR pathwayJing Gao0Xiaojuan Lu1 Guanglei Wang2Tanling Huang3Zhongyu Tuo4Weiwei Meng5Clinical Laboratory, ShenZhen Baoan Shiyan People’s Hospital, Guangdong Province, ChinaClinical Laboratory, ShenZhen Baoan Shiyan People’s Hospital, Guangdong Province, ChinaClinical Laboratory, ShenZhen Baoan Shiyan People’s Hospital, Guangdong Province, ChinaClinical Laboratory, ShenZhen Baoan Shiyan People’s Hospital, Guangdong Province, ChinaClinical Laboratory, ShenZhen Baoan Shiyan People’s Hospital, Guangdong Province, ChinaShenZhen Baoan Shiyan People’s HospitalDiffuse large B-cell lymphoma (DLBCL) is a highly heterogeneous metastatic lymphoma that can be treated by targeting angiogenesis. Apolipoprotein C1 (APOC1) plays a significant role in the proliferation and metastasis of various malignant tumors; however, its role in DLBCL—particularly its effects on angiogenesis—remains largely unexplored. This study investigates the correlation between APOC1 expression and patient prognosis in DLBCL. Using APOC1 gene knockdown, apoptosis, migration, and invasion were assessed through flow cytometry, the EDU assay, wound healing, and Transwell assays. Additionally, human umbilical vein endothelial cells (HUVEC) angiogenesis was evaluated. Advanced techniques, such as immunofluorescence, TUNEL assay, and immunohistochemical labeling were employed to analyze the effects of APOC1 knockdown on the PI3K/AKT/mTOR signaling pathway and tumor formation in nude mice. Results showed that APOC1 is overexpressed in DLBCL tissues and cells, with high APOC1 levels associated with poor patient prognosis. In vitro experiments revealed that APOC1 knockdown increased apoptosis and inhibited cell proliferation, migration, invasion, HUVEC angiogenesis, and PI3K/AKT/mTOR signaling pathway protein expression in DLBCL cells. Similarly, in vivo studies demonstrated that APOC1 knockdown significantly reduced tumor growth, angiogenesis-related proteins, and phosphorylated PI3K/AKT/mTOR pathway proteins in nude mice. APOC1 knockdown promotes apoptosis and suppresses angiogenesis in DLBCL cells by inhibiting the PI3K/AKT/mTOR pathway. https://bjbms.org/ojs/index.php/bjbms/article/view/11550Diffuse large B-cell lymphomaDLBCLApolipoprotein C1APOC1human umbilical vein endothelial cellsHUVECs
spellingShingle Jing Gao
Xiaojuan Lu
Guanglei Wang
Tanling Huang
Zhongyu Tuo
Weiwei Meng
APOC1 knockdown induces apoptosis and decreases angiogenesis in diffuse large B-cell lymphoma cells through blocking the PI3K/AKT/mTOR pathway
Biomolecules & Biomedicine
Diffuse large B-cell lymphoma
DLBCL
Apolipoprotein C1
APOC1
human umbilical vein endothelial cells
HUVECs
title APOC1 knockdown induces apoptosis and decreases angiogenesis in diffuse large B-cell lymphoma cells through blocking the PI3K/AKT/mTOR pathway
title_full APOC1 knockdown induces apoptosis and decreases angiogenesis in diffuse large B-cell lymphoma cells through blocking the PI3K/AKT/mTOR pathway
title_fullStr APOC1 knockdown induces apoptosis and decreases angiogenesis in diffuse large B-cell lymphoma cells through blocking the PI3K/AKT/mTOR pathway
title_full_unstemmed APOC1 knockdown induces apoptosis and decreases angiogenesis in diffuse large B-cell lymphoma cells through blocking the PI3K/AKT/mTOR pathway
title_short APOC1 knockdown induces apoptosis and decreases angiogenesis in diffuse large B-cell lymphoma cells through blocking the PI3K/AKT/mTOR pathway
title_sort apoc1 knockdown induces apoptosis and decreases angiogenesis in diffuse large b cell lymphoma cells through blocking the pi3k akt mtor pathway
topic Diffuse large B-cell lymphoma
DLBCL
Apolipoprotein C1
APOC1
human umbilical vein endothelial cells
HUVECs
url https://bjbms.org/ojs/index.php/bjbms/article/view/11550
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