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Extract Formulation of Zingiber officinale and Phylanthus reticulatus Induces Apoptosis of WiDr Colon Cancer Cells

Biosaintifika: Journal of Biology & Biology Education · Vol. 17 No. 3 (2025) · pp. 370–381

DOI
10.15294/biosaintifika.v17i3.25776
ISSN
2338-7610, 2085-191X
Published
2025-11-18
Publisher
Universitas Negeri Semarang
Language
eng

Abstract

People use ginger (Zingiber officinale) extensively for health purposes. Our previous studies have shown that Phyllanthus reticulatus has strong antioxidant capabilities. This study investigates the anticancer potential of ethanolic extract of Z. officinale and P. reticulatus formulations (ZP), focusing on their cytotoxicity and mechanisms against cancer cells. Samples were extracted using the maceration method. The method for determining the cytotoxicity of cells is MTT, the cell cycle is flow cytometry, apoptotic cells are flow cytometry and double staining, and caspase-8 and caspase-9 expression using the immunocytochemistry method. The analysis of caspase-8 and caspase-9 expression using the immunocytochemistry method. Among the tested formulations, the ethanolic extract of ZP_1:0 showed the most promise against WiDr colon cancer cells (IC50 value of 102.1 µg/ml). The ZP_1:0 demonstrated dose-dependent apoptosis induction in WiDr cells, showing early and late apoptosis, with minimal necrosis. The extract activates extrinsic and intrinsic apoptotic pathways in inducing cancer cell death. Compared to doxorubicin, the ZP 1:0 formulation selectively promotes apoptosis with reduced necrotic damage, suggesting the potential for reduced systemic toxicity. The study supports the potential of Z. officinale as a source of safer, plant-based anticancer agents, particularly for colon cancer, while recommending further research to identify and enhance active compounds.

Keywords

Collaboration network of the authors

40 authors · 277 co-authorship links

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  • Chaoyang University of Technology
  • Affiliation unknown
  • Different organisations
  • Same organisation
  • Affiliation unknown
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Co-authorOrganisationJoint articles
Andreas B.A. SukmanaAffiliation unknown2
Sucahyo SucahyoAffiliation unknown2
Desti C. CahyaningrumAffiliation unknown2
Susanti P. HastutiAffiliation unknown2
Cocok A.M. BerutuAffiliation unknown2
Risky H. PoluanAffiliation unknown2
Natalia R. KeliatAffiliation unknown2
Risya P. SitumorangAffiliation unknown2
Elizabeth B.E. KristianiAffiliation unknown2
V. I. MeitiniartiAffiliation unknown2
Rully A. NugrohoAffiliation unknown2
Agna S. KraveAffiliation unknown2
Otilda Fátima AraújoAffiliation unknown2
Laurentius Hartanto NugrohoAffiliation unknown2
Evangs MailoaAffiliation unknown1
Radius TanoneChaoyang University of Technology1
Krismiyati KrismiyatiAffiliation unknown1
Budhi KristiantoAffiliation unknown1
Erwien ChristiantoAffiliation unknown1
Andreas A. SukmanaAffiliation unknown1
Betty E. KristianiAffiliation unknown1
Hindriyanto D. PurnomoAffiliation unknown1
Teguh I. BayuAffiliation unknown1
Adi NugrohoAffiliation unknown1
Hanita YuliaAffiliation unknown1
Marisa C. TapilouwAffiliation unknown1
Djohan DjohanAffiliation unknown1
Marchella G. PutriciaAffiliation unknown1
Easter G. TuandaliAffiliation unknown1
Ciputra S. MangesaAffiliation unknown1
Shabrina R.A. FernandaAffiliation unknown1
Imel T.Y. ZebuaAffiliation unknown1
Sheina Revania Putri DooAffiliation unknown1
Samse PandianganAffiliation unknown1
Siti Nur HidayatiAffiliation unknown1
V. Irene MeitiniartiAffiliation unknown1

Affiliations come from OpenAlex; journal OAI-PMH metadata carries none. Authors without an OpenAlex ID are matched by name, which can merge or split people.

Metadata source: OAI-PMH (metadata jurnal) https://journal.unnes.ac.id/journals/biosaintifika/oai, first harvested 5 Nov 2026, last seen 5 Nov 2026.
Original metadata (oai_dc)
<oai_dc:dc xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/  http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
	<dc:title xml:lang="en">Extract Formulation of Zingiber officinale and Phylanthus reticulatus Induces Apoptosis of WiDr Colon Cancer Cells</dc:title>
	<dc:creator xml:lang="en">Kristiani, Elizabeth Betty Elok</dc:creator>
	<dc:creator xml:lang="en">Kasmiyati, Sri </dc:creator>
	<dc:creator xml:lang="en">Martono, Yohanes </dc:creator>
	<dc:creator xml:lang="en">Kachingwe, Baxter Hepburn </dc:creator>
	<dc:subject xml:lang="en">Caspase</dc:subject>
	<dc:subject xml:lang="en">cell cycle</dc:subject>
	<dc:subject xml:lang="en">cytotoxicity assay</dc:subject>
	<dc:subject xml:lang="en">Phyllanthus reticulatus</dc:subject>
	<dc:subject xml:lang="en">Zingiber officinale</dc:subject>
	<dc:description xml:lang="en">People use ginger (Zingiber officinale) extensively for health purposes. Our previous studies have shown that Phyllanthus reticulatus has strong antioxidant capabilities. This study investigates the anticancer potential of ethanolic extract of Z. officinale and P. reticulatus formulations (ZP), focusing on their cytotoxicity and mechanisms against cancer cells. Samples were extracted using the maceration method. The method for determining the cytotoxicity of cells is MTT, the cell cycle is flow cytometry, apoptotic cells are flow cytometry and double staining, and caspase-8 and caspase-9 expression using the immunocytochemistry method. The analysis of caspase-8 and caspase-9 expression using the immunocytochemistry method. Among the tested formulations, the ethanolic extract of ZP_1:0 showed the most promise against WiDr colon cancer cells (IC50 value of 102.1 µg/ml). The ZP_1:0 demonstrated dose-dependent apoptosis induction in WiDr cells, showing early and late apoptosis, with minimal necrosis. The extract activates extrinsic and intrinsic apoptotic pathways in inducing cancer cell death. Compared to doxorubicin, the ZP 1:0 formulation selectively promotes apoptosis with reduced necrotic damage, suggesting the potential for reduced systemic toxicity. The study supports the potential of Z. officinale as a source of safer, plant-based anticancer agents, particularly for colon cancer, while recommending further research to identify and enhance active compounds.</dc:description>
	<dc:publisher xml:lang="en">Universitas Negeri Semarang</dc:publisher>
	<dc:date>2025-11-18</dc:date>
	<dc:type>info:eu-repo/semantics/article</dc:type>
	<dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
	<dc:type xml:lang="en">Peer-reviewed Article</dc:type>
	<dc:format>application/pdf</dc:format>
	<dc:identifier>https://journal.unnes.ac.id/journals/biosaintifika/article/view/25776</dc:identifier>
	<dc:identifier>10.15294/biosaintifika.v17i3.25776</dc:identifier>
	<dc:source xml:lang="en">Biosaintifika: Journal of Biology &amp; Biology Education; Vol. 17 No. 3 (2025): November 2025; 370-381</dc:source>
	<dc:source>2338-7610</dc:source>
	<dc:source>2085-191X</dc:source>
	<dc:source>10.15294/biosaintifika.v17i3</dc:source>
	<dc:language>eng</dc:language>
	<dc:relation>https://journal.unnes.ac.id/journals/biosaintifika/article/view/25776/7065</dc:relation>
	<dc:rights xml:lang="en">Copyright (c) 2025 Biosaintifika: Journal of Biology &amp; Biology Education</dc:rights>
</oai_dc:dc>