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Updated: Mar 31, 2026

Long-term Live-cell Imaging to Assess Cell Fate in Response to Paclitaxel
Published on: May 14, 2018
[Chemotherapy with paclitaxel leads to microRNA release]
R Maushagen1, R Pries, B Wollenberg
1Klinik und Poliklinik für Hals-, Nasen- und Ohrenheilkunde, Universitätsklinikum Schleswig-Holstein, Campus Lübeck, Lübeck, Germany
Background:
During recent years, microRNAs (Greek: micros = small; miRNA) have become more important. miRNAs are highly conserved, noncoding, single-stranded RNA molecules 17–28 nucleotide in length. Secreted by tumor cells, miRNAs regulate many biological processes and are also involved in chemoresistance. Classical forms of cancer treatment lead to miRNA release. Which miRNAs are correlated to head and neck squamous cell carcinomas (HNSCC) and their chemoresistance to paclitaxel remains unknown.
Objectives:
Identification of miRNAs expressed in HNSCC and elucidation of those involved in conferring chemoresistance to paclitaxel.
Materials And Methods:
To identify changes in gene expression, HNSCC cell lines were treated with 10 μM paclitaxel for 48 h and analyzed by microarray analysis. Thereafter, changed in expression of single miRNAs (miR221*, miR222 and miR222*) following paclitaxel treatment were analyzed using a quantitative real-time polymerase chain reaction (qRT-PCR).
Results:
Under treatment with paclitaxel, miRNAs were released. The dominant change is upregulation of MIR222 gene expression. Regulation of miR222* expression under paclitaxel treatment seems to be different in human papillomavirus (HPV)-negative and HPV-positive HNSCC cell lines.
Conclusion:
Expression of mirR221/222 is correlated to cell cycle regulation, carcinogenesis, and chemoresistance. Detailed knowledge of the molecular mechanisms and effects ofmiRNAs is important for identifying miRNAs as cancermarkers, as well as for increasing the efficiency of cancer therapeutics.
Insights
MicroRNAs (miRNAs) are linked to head and neck squamous cell carcinomas (HNSCC) and chemoresistance. Paclitaxel treatment upregulates MIR222 gene expression, impacting HNSCC chemoresistance.
Area of Science:
- Molecular biology
- Cancer research
- Biochemistry
Background:
- MicroRNAs (miRNAs) are small, noncoding RNA molecules crucial in biological processes and chemoresistance.
- Tumor-secreted miRNAs play a role in cancer progression and treatment resistance.
- The specific miRNAs involved in head and neck squamous cell carcinomas (HNSCC) and paclitaxel chemoresistance are not well understood.
Purpose of the Study:
- To identify miRNAs expressed in HNSCC.
- To elucidate the role of specific miRNAs in paclitaxel chemoresistance in HNSCC.
Main Methods:
- HNSCC cell lines were treated with paclitaxel (10 μM for 48 h).
- Gene expression changes were analyzed using microarray analysis.
- Quantitative real-time polymerase chain reaction (qRT-PCR) was used to analyze specific miRNA expression (miR221*, miR222, miR222*).
Main Results:
- Paclitaxel treatment led to miRNA release.
- A significant upregulation of MIR222 gene expression was observed.
- The regulation of miR222* expression differed between HPV-negative and HPV-positive HNSCC cell lines.
Conclusions:
- miRNA expression, specifically miR221/222, is correlated with cell cycle regulation, carcinogenesis, and chemoresistance.
- Understanding miRNA mechanisms is vital for developing novel cancer biomarkers.
- Targeting miRNAs could enhance the efficacy of cancer therapeutics.
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