Targeting the integrin beta 1‐focal adhesion kinase axis with artemisinin: Biophysical disruption of cell adhesion, migration, and invasion in tongue cancer Article Swipe
Laurensia Danis Anggradita
,
Joo-Hyun Kim
,
Min‐Kyu Kim
,
Ji Won Son
,
Mohd Farhan
,
Jothilin Subitsha Alex Jeberson
,
Ali Taghizadeh
,
Hae‐Won Kim
,
Jae Hong Park
,
Jaemoon Yang
,
Hyung Kwon Byeon
,
Sung Sik Hur
,
Myung Jin Ban
,
Yongsung Hwang
·
YOU?
·
· 2025
· Open Access
·
· DOI: https://doi.org/10.1002/viw.20240089
YOU?
·
· 2025
· Open Access
·
· DOI: https://doi.org/10.1002/viw.20240089
Tongue cancer is a significant threat to human health due to its propensity to spread throughout the oral cavity and to other regions of the head and neck. The challenges posed by its high invasion, metastasis, and late clinical detection underscore the urgency for effective clinical interventions. In this study, we elucidate the promising anti‐cancer properties of artemisinin, an anti‐malarial drug, in inhibiting cellular interactions within a tongue cancer cell line. Our findings reveal that artemisinin treatment effectively suppresses phosphorylated focal adhesion kinase and its downstream AKT pathway, thereby enhancing apoptotic processes and inducing cell cycle arrest, consequently impeding cellular proliferation. Moreover, artemisinin treatment induces focal adhesion rearrangement and diminishes the cell's capacity to generate traction stress, consequently restraining cell migration on the matrix, as determined via traction force microscopy. Additionally, a transition from N‐cadherin to E‐cadherin expression occurs at cellular junctions, lowering intracellular stress, as measured by monolayer stress microscopy. This transition significantly curtails cellular migratory capabilities. Our in vivo studies corroborate these findings, showing a significant reduction in tumor volume following artemisinin treatment. Our study highlights the therapeutic potential of artemisinin use as a novel strategy for tongue cancer treatment, which acts via modulating both intracellular and intercellular interactions.
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Metadata
- Type
- article
- Language
- en
- Landing Page
- https://doi.org/10.1002/viw.20240089
- https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/VIW.20240089
- OA Status
- gold
- Cited By
- 1
- References
- 87
- Related Works
- 10
- OpenAlex ID
- https://openalex.org/W4409176657
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Raw OpenAlex JSON
- OpenAlex ID
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https://openalex.org/W4409176657Canonical identifier for this work in OpenAlex
- DOI
-
https://doi.org/10.1002/viw.20240089Digital Object Identifier
- Title
-
Targeting the integrin beta 1‐focal adhesion kinase axis with artemisinin: Biophysical disruption of cell adhesion, migration, and invasion in tongue cancerWork title
- Type
-
articleOpenAlex work type
- Language
-
enPrimary language
- Publication year
-
2025Year of publication
- Publication date
-
2025-04-01Full publication date if available
- Authors
-
Laurensia Danis Anggradita, Joo-Hyun Kim, Min‐Kyu Kim, Ji Won Son, Mohd Farhan, Jothilin Subitsha Alex Jeberson, Ali Taghizadeh, Hae‐Won Kim, Jae Hong Park, Jaemoon Yang, Hyung Kwon Byeon, Sung Sik Hur, Myung Jin Ban, Yongsung HwangList of authors in order
- Landing page
-
https://doi.org/10.1002/viw.20240089Publisher landing page
- PDF URL
-
https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/VIW.20240089Direct link to full text PDF
- Open access
-
YesWhether a free full text is available
- OA status
-
goldOpen access status per OpenAlex
- OA URL
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https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/VIW.20240089Direct OA link when available
- Concepts
-
Integrin, Focal adhesion, Adhesion, Artemisinin, Cell adhesion, Cell biology, Tongue, Cancer, Chemistry, Cell migration, Cell adhesion molecule, Cancer research, Cell, Biology, Immunology, Medicine, Biochemistry, Pathology, Signal transduction, Genetics, Plasmodium falciparum, Organic chemistry, MalariaTop concepts (fields/topics) attached by OpenAlex
- Cited by
-
1Total citation count in OpenAlex
- Citations by year (recent)
-
2025: 1Per-year citation counts (last 5 years)
- References (count)
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87Number of works referenced by this work
- Related works (count)
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10Other works algorithmically related by OpenAlex
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| abstract_inverted_index.studies | 162 |
| abstract_inverted_index.thereby | 89 |
| abstract_inverted_index.urgency | 43 |
| abstract_inverted_index.Abstract | 0 |
| abstract_inverted_index.adhesion | 82, 107 |
| abstract_inverted_index.capacity | 113 |
| abstract_inverted_index.cellular | 64, 100, 141, 156 |
| abstract_inverted_index.clinical | 39, 46 |
| abstract_inverted_index.curtails | 155 |
| abstract_inverted_index.findings | 73 |
| abstract_inverted_index.generate | 115 |
| abstract_inverted_index.impeding | 99 |
| abstract_inverted_index.inducing | 94 |
| abstract_inverted_index.lowering | 143 |
| abstract_inverted_index.measured | 147 |
| abstract_inverted_index.pathway, | 88 |
| abstract_inverted_index.strategy | 188 |
| abstract_inverted_index.traction | 116, 128 |
| abstract_inverted_index.Moreover, | 102 |
| abstract_inverted_index.apoptotic | 91 |
| abstract_inverted_index.detection | 40 |
| abstract_inverted_index.effective | 45 |
| abstract_inverted_index.elucidate | 52 |
| abstract_inverted_index.enhancing | 90 |
| abstract_inverted_index.findings, | 165 |
| abstract_inverted_index.following | 173 |
| abstract_inverted_index.invasion, | 35 |
| abstract_inverted_index.migration | 121 |
| abstract_inverted_index.migratory | 157 |
| abstract_inverted_index.monolayer | 149 |
| abstract_inverted_index.potential | 181 |
| abstract_inverted_index.processes | 92 |
| abstract_inverted_index.promising | 54 |
| abstract_inverted_index.reduction | 169 |
| abstract_inverted_index.treatment | 77, 104 |
| abstract_inverted_index.challenges | 30 |
| abstract_inverted_index.determined | 126 |
| abstract_inverted_index.diminishes | 110 |
| abstract_inverted_index.downstream | 86 |
| abstract_inverted_index.expression | 138 |
| abstract_inverted_index.highlights | 178 |
| abstract_inverted_index.inhibiting | 63 |
| abstract_inverted_index.junctions, | 142 |
| abstract_inverted_index.modulating | 196 |
| abstract_inverted_index.propensity | 13 |
| abstract_inverted_index.properties | 56 |
| abstract_inverted_index.suppresses | 79 |
| abstract_inverted_index.throughout | 16 |
| abstract_inverted_index.transition | 133, 153 |
| abstract_inverted_index.treatment, | 192 |
| abstract_inverted_index.treatment. | 175 |
| abstract_inverted_index.underscore | 41 |
| abstract_inverted_index.artemisinin | 76, 103, 174, 183 |
| abstract_inverted_index.corroborate | 163 |
| abstract_inverted_index.effectively | 78 |
| abstract_inverted_index.metastasis, | 36 |
| abstract_inverted_index.microscopy. | 130, 151 |
| abstract_inverted_index.restraining | 119 |
| abstract_inverted_index.significant | 5, 168 |
| abstract_inverted_index.therapeutic | 180 |
| abstract_inverted_index.E‐cadherin | 137 |
| abstract_inverted_index.N‐cadherin | 135 |
| abstract_inverted_index.artemisinin, | 58 |
| abstract_inverted_index.consequently | 98, 118 |
| abstract_inverted_index.interactions | 65 |
| abstract_inverted_index.Additionally, | 131 |
| abstract_inverted_index.anti‐cancer | 55 |
| abstract_inverted_index.capabilities. | 158 |
| abstract_inverted_index.interactions. | 201 |
| abstract_inverted_index.intercellular | 200 |
| abstract_inverted_index.intracellular | 144, 198 |
| abstract_inverted_index.rearrangement | 108 |
| abstract_inverted_index.significantly | 154 |
| abstract_inverted_index.interventions. | 47 |
| abstract_inverted_index.phosphorylated | 80 |
| abstract_inverted_index.proliferation. | 101 |
| abstract_inverted_index.anti‐malarial | 60 |
| cited_by_percentile_year.max | 95 |
| cited_by_percentile_year.min | 91 |
| countries_distinct_count | 1 |
| institutions_distinct_count | 14 |
| citation_normalized_percentile.value | 0.85168583 |
| citation_normalized_percentile.is_in_top_1_percent | False |
| citation_normalized_percentile.is_in_top_10_percent | True |