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Computational Design of siRNA Targeting Homo sapiens HER2 Splice Variant mRNA: A Potential Strategy for Breast Cancer Intervention

Biosaintifika: Journal of Biology & Biology Education · Vol. 16 No. 3 (2024) · hlm. 384–393

DOI
10.15294/biosaintifika.v16i3.3685
ISSN
2338-7610, 2085-191X
Terbit
2024-12-24
Penerbit
Universitas Negeri Semarang
Bahasa
eng

Abstrak

This research focuses on an innovative approach utilizing in silico methods to design small interfering RNA (siRNA) targeting the HER2 splice variant mRNA in Homo sapiens. HER2 is known to be overexpressed in certain types of breast cancer, contributing to tumor progression and poor prognosis. By designing siRNA molecules that can specifically bind to and degrade HER2 mRNA, this study aims to reduce HER2 protein levels, thereby hindering the growth and spread of breast cancer cells. The in-silico design process involves identifying optimal siRNA sequences that maximize target specificity and minimize off-target effects, which is crucial for potential therapeutic applications. This approach represents a promising step towards personalized medicine in the treatment of breast cancer, offering a targeted strategy to combat this variant associated with aggressive disease. The methodology comprises the RNA computational tools used for the design, the selection criteria for siRNA candidates, and the potential implications of this research in a clinical setting. The resulting outcomes are 2D and 3D siRNA designs that could potentially silence HER2 mRNA through an in-silico approach. The leads were generated using a de novo modeling approach, with no existing template available in GenBank. Moreover, it is concluded that computational tools can generate sufficiently stable 2D and 3D RNA models that could be advanced for further molecular simulation studies. The benefit of this outcome is that it facilitates better preparation for wet laboratory experiments in siRNA assays, with future implementation in vivo and clinical trial settings.

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  • Universitas Airlangga
  • Indonesia International Institute for Life Sciences
  • University of Nusa Cendana
  • Universitas Negeri Padang
  • Russian State Agrarian University - Moscow Timiryazev Agricultural Academy
  • Yaroslav-the-Wise Novgorod State University
  • Universitas Gadjah Mada
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Rekan penulisOrganisasiArtikel bersama
Rizky NurdiansyahIndonesia International Institute for Life Sciences2
Fredy Z. SaudaleUniversity of Nusa Cendana1
Reinner Ishaq LerrickUniversity of Nusa Cendana1
F. MaritiAfiliasi tidak diketahui1
Mochammad Aqilah HerdiansyahUniversitas Airlangga1
Arif Nur Muhammad AnsoriUniversitas Airlangga1
Mochamad Radika Tory AlifiansyahUniversitas Airlangga1
Dhea AnggrainiUniversitas Airlangga1
Qiara Amelia Putri PriyonoUniversitas Airlangga1
Putri Antika YusniasariUniversitas Airlangga1
Amelia Julia Tria FettyUniversitas Airlangga1
Rahadian ZainulUniversitas Negeri Padang1
Maksim RebezovAfiliasi tidak diketahui1
Evgeniy KolesnikRussian State Agrarian University - Moscow Timiryazev Agricultural Academy1
Nikolai MaksimiukYaroslav-the-Wise Novgorod State University1
Alexander Patera NugrahaUniversitas Airlangga1
Santika Lusia UtamiUniversitas Gadjah Mada1
Wahyu Choirur RizkySulaiman Al Rajhi Colleges1
Tim Godefridus Antonius DingsMaastricht University1
Md. Emdad UllahMississippi State University1
Vikash JakhmolaUttaranchal University1
Imron ImronPoliteknik Pertanian Negeri Samarinda1
David AgustriawanUniversitas Amikom Yogyakarta1
Adhityo WicaksonoAfiliasi tidak diketahui1
Didik Huswo UtomoNagoya University1
Nihayatul KarimahIndonesia International Institute for Life Sciences1
Jeremias IvanIndonesia International Institute for Life Sciences1
Rico Alexander PratamaIndonesia International Institute for Life Sciences1
Junaida AstinaIndonesia International Institute for Life Sciences1
Mufasirin MufasirinUniversitas Airlangga1
Kusnoto KusnotoUniversitas Airlangga1
Lucia Tri SuwantiUniversitas Airlangga1
Poedji HastutiekUniversitas Airlangga1
Endang SuprihatiUniversitas Airlangga1
Aswin Rafif KhairullahNational Research and Innovation Agency1
Yulianna PuspitasariUniversitas Airlangga1
Muhammad ‘Ahdi KurniawanUniversitas Airlangga1

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Sumber metadata: OAI-PMH (metadata jurnal) https://journal.unnes.ac.id/journals/biosaintifika/oai, pertama di-harvest 5 Nov 2026, terakhir terlihat 8 Nov 2026.
Metadata asli (oai_dc)
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	<dc:title xml:lang="en">Computational Design of siRNA Targeting Homo sapiens HER2 Splice Variant mRNA: A Potential Strategy for Breast Cancer Intervention</dc:title>
	<dc:creator xml:lang="en">Parikesit, Arli Aditya</dc:creator>
	<dc:creator xml:lang="en">Ansori, Arif Nur Muhammad</dc:creator>
	<dc:creator xml:lang="en">Kharisma, Viol Dhea</dc:creator>
	<dc:subject xml:lang="en"> Breast Cancer</dc:subject>
	<dc:subject xml:lang="en">computational tools</dc:subject>
	<dc:subject xml:lang="en">HER2</dc:subject>
	<dc:subject xml:lang="en">siRNA</dc:subject>
	<dc:subject xml:lang="en">mRNA</dc:subject>
	<dc:description xml:lang="en">This research focuses on an innovative approach utilizing in silico methods to design small interfering RNA (siRNA) targeting the HER2 splice variant mRNA in Homo sapiens. HER2 is known to be overexpressed in certain types of breast cancer, contributing to tumor progression and poor prognosis. By designing siRNA molecules that can specifically bind to and degrade HER2 mRNA, this study aims to reduce HER2 protein levels, thereby hindering the growth and spread of breast cancer cells. The in-silico design process involves identifying optimal siRNA sequences that maximize target specificity and minimize off-target effects, which is crucial for potential therapeutic applications. This approach represents a promising step towards personalized medicine in the treatment of breast cancer, offering a targeted strategy to combat this variant associated with aggressive disease. The methodology comprises the RNA computational tools used for the design, the selection criteria for siRNA candidates, and the potential implications of this research in a clinical setting. The resulting outcomes are 2D and 3D siRNA designs that could potentially silence HER2 mRNA through an in-silico approach. The leads were generated using a de novo modeling approach, with no existing template available in GenBank. Moreover, it is concluded that computational tools can generate sufficiently stable 2D and 3D RNA models that could be advanced for further molecular simulation studies. The benefit of this outcome is that it facilitates better preparation for wet laboratory experiments in siRNA assays, with future implementation in vivo and clinical trial settings.</dc:description>
	<dc:publisher xml:lang="en">Universitas Negeri Semarang</dc:publisher>
	<dc:date>2024-12-24</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/3685</dc:identifier>
	<dc:identifier>10.15294/biosaintifika.v16i3.3685</dc:identifier>
	<dc:source xml:lang="en">Biosaintifika: Journal of Biology &amp; Biology Education; Vol. 16 No. 3 (2024): December 2024; 384-393</dc:source>
	<dc:source>2338-7610</dc:source>
	<dc:source>2085-191X</dc:source>
	<dc:source>10.15294/biosaintifika.v16i3</dc:source>
	<dc:language>eng</dc:language>
	<dc:relation>https://journal.unnes.ac.id/journals/biosaintifika/article/view/3685/2224</dc:relation>
	<dc:rights xml:lang="en">Copyright (c) 2024 Biosaintifika: Journal of Biology &amp; Biology Education</dc:rights>
</oai_dc:dc>