Andrographolide suppresses cervical cancer progression by targeting angiogenesis and inducing apoptosis in a CAM-PDX model

Cervical cancer poses significant clinical challenges, particularly in advanced stages. This study explores the therapeutic potential of andrographolide (AND), a bioactive compound derived from Andrographis paniculata, in mitigating cervical cancer progression using the chick embryo chorioallantoic...

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Main Authors: Wanwan Zou, Jun Lou, Yun Yi, Yiming Cui, Xiaoyan Chu
Format: Article
Language:English
Published: Association of Basic Medical Sciences of Federation of Bosnia and Herzegovina 2025-02-01
Series:Biomolecules & Biomedicine
Subjects:
Online Access:https://www.bjbms.org/ojs/index.php/bjbms/article/view/11432
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author Wanwan Zou
Jun Lou
Yun Yi
Yiming Cui
Xiaoyan Chu
author_facet Wanwan Zou
Jun Lou
Yun Yi
Yiming Cui
Xiaoyan Chu
author_sort Wanwan Zou
collection DOAJ
description Cervical cancer poses significant clinical challenges, particularly in advanced stages. This study explores the therapeutic potential of andrographolide (AND), a bioactive compound derived from Andrographis paniculata, in mitigating cervical cancer progression using the chick embryo chorioallantoic membrane patient-derived xenograft (CAM-PDX) model. The model was validated through hematoxylin-eosin staining and immunohistochemistry, which confirmed its ability to accurately replicate the histological and molecular characteristics of patient-derived xenografts, establishing its reliability for therapeutic screening. A dose of 20 mg/kg AND was selected for further evaluation based on preliminary CAM assay findings. In the CAM-PDX model, AND significantly inhibited tumor growth, primarily by reducing angiogenesis and vessel density. Immunohistochemical analysis revealed that AND downregulated key proteins associated with cancer cell proliferation and survival, including Ki67, B-cell lymphoma 2 (BCL-2), and Erythroblast transformation-specific-related gene (ERG). These results indicate that AND not only disrupts tumor angiogenesis but also induces cell cycle arrest and promotes apoptosis in cervical cancer cells. In summary, this study successfully established a reproducible CAM-PDX model for drug evaluation and highlighted the potential of AND as a promising therapeutic candidate for cervical cancer, warranting further clinical investigation.
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institution Kabale University
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spelling doaj-art-f7b497495f724dd395047aae5a9e504a2025-02-11T16:43:08ZengAssociation of Basic Medical Sciences of Federation of Bosnia and HerzegovinaBiomolecules & Biomedicine2831-08962831-090X2025-02-0110.17305/bb.2025.11432Andrographolide suppresses cervical cancer progression by targeting angiogenesis and inducing apoptosis in a CAM-PDX modelWanwan Zou0Jun Lou1Yun Yi2Yiming Cui3Xiaoyan Chu4https://orcid.org/0009-0000-7258-6176Jiangxi Provincial Cancer HospitalDepartment of Gynecological Oncology, Jiangxi Provincial Cancer Hospital, Nanchang, ChinaDepartment of Gynecological Oncology, Jiangxi Provincial Cancer Hospital, Nanchang, ChinaDepartment of Mathematics, Applied Mathematics and Statistics, Case Western Reserve University, Cleveland, USADepartment of Gynecological Oncology, Jiangxi Provincial Cancer Hospital, Nanchang, China Cervical cancer poses significant clinical challenges, particularly in advanced stages. This study explores the therapeutic potential of andrographolide (AND), a bioactive compound derived from Andrographis paniculata, in mitigating cervical cancer progression using the chick embryo chorioallantoic membrane patient-derived xenograft (CAM-PDX) model. The model was validated through hematoxylin-eosin staining and immunohistochemistry, which confirmed its ability to accurately replicate the histological and molecular characteristics of patient-derived xenografts, establishing its reliability for therapeutic screening. A dose of 20 mg/kg AND was selected for further evaluation based on preliminary CAM assay findings. In the CAM-PDX model, AND significantly inhibited tumor growth, primarily by reducing angiogenesis and vessel density. Immunohistochemical analysis revealed that AND downregulated key proteins associated with cancer cell proliferation and survival, including Ki67, B-cell lymphoma 2 (BCL-2), and Erythroblast transformation-specific-related gene (ERG). These results indicate that AND not only disrupts tumor angiogenesis but also induces cell cycle arrest and promotes apoptosis in cervical cancer cells. In summary, this study successfully established a reproducible CAM-PDX model for drug evaluation and highlighted the potential of AND as a promising therapeutic candidate for cervical cancer, warranting further clinical investigation. https://www.bjbms.org/ojs/index.php/bjbms/article/view/11432Cervical cancerandrographolideANDangiogenesis inhibitionchorioallantoic membrane patient-derived xenograftCAM-PDX
spellingShingle Wanwan Zou
Jun Lou
Yun Yi
Yiming Cui
Xiaoyan Chu
Andrographolide suppresses cervical cancer progression by targeting angiogenesis and inducing apoptosis in a CAM-PDX model
Biomolecules & Biomedicine
Cervical cancer
andrographolide
AND
angiogenesis inhibition
chorioallantoic membrane patient-derived xenograft
CAM-PDX
title Andrographolide suppresses cervical cancer progression by targeting angiogenesis and inducing apoptosis in a CAM-PDX model
title_full Andrographolide suppresses cervical cancer progression by targeting angiogenesis and inducing apoptosis in a CAM-PDX model
title_fullStr Andrographolide suppresses cervical cancer progression by targeting angiogenesis and inducing apoptosis in a CAM-PDX model
title_full_unstemmed Andrographolide suppresses cervical cancer progression by targeting angiogenesis and inducing apoptosis in a CAM-PDX model
title_short Andrographolide suppresses cervical cancer progression by targeting angiogenesis and inducing apoptosis in a CAM-PDX model
title_sort andrographolide suppresses cervical cancer progression by targeting angiogenesis and inducing apoptosis in a cam pdx model
topic Cervical cancer
andrographolide
AND
angiogenesis inhibition
chorioallantoic membrane patient-derived xenograft
CAM-PDX
url https://www.bjbms.org/ojs/index.php/bjbms/article/view/11432
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