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Updated: Mar 26, 2026

In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice
Published on: August 23, 2019
siRNA targeting RBP2 inhibits expression, proliferation, tumorigenicity and invasion in thyroid carcinoma cells
Ling-Ling Kong1, Dong-Mei Man2, Tian Wang3
1Department of Pathology, Basic Science School, Jining Medical University, Jining, Shandong 272067, P.R. China.
Abstract:
In order to estimate the effects of small interfering RNA (siRNA) targeting retinoblastoma binding protein 2 (RBP2) on the proliferation, expression, invasion, migration and tumorigenicity abilities of papillary thyroid carcinoma K1 cells, siRNA targeting RBP2 (RBP2-siRNA) and negative control siRNA were transfected into K1 cells. The mRNA levels of RBP2 in the transfected cells were estimated by reverse transcription-quantitative polymerase chain reaction (RT-qPCR), and the protein levels of RBP2 in these cells were evaluated by western blot analysis and immunocytochemical (ICC) analyses. The growth, tumorigenicity, migration and invasion abilities of the transfected cells were measured by Cell Counting Kit-8 (CCK-8), soft agar colony formation and transwell chamber assay, respectively. The ICC results demonstrated that the protein expression levels of RBP2 were lower in the RBP2-siRNA-transfected cells than in the blank and control cells (analysis of variance, F=26.754, P<0.01). RBP2-siRNA downregulated RBP2 at the mRNA (t=8.869) and protein level (F=60.835) (P=0.000 vs. control cells). In addition, the transfection of RBP2-siRNA into K1 cells also suppressed cell proliferation at 24, 48 and 72 h post-transfection (t=7.650, P<0.01; t=2.606, P=0.016; and t=2.377, P=0.027, respectively). Compared with the control group, the number of invasive and migrated cells were significantly reduced in the RBP2-siRNA-transfected group (t=4.774 and t=6.366, respectively; P<0.01). Furthermore, the tumorigenic potential of the cells transfected with RBP2-siRNA was markedly reduced, as indicated by the soft agar formation assay (t=2.749, P=0.014 vs. control cells). In conclusion, the transfection of RBP2-siRNA into papillary thyroid carcinoma K1 cells suppressed the expression of RBP2 in these cells, and reduced their proliferation, invasion, migration and tumorigenic potential. Therefore, targeting RBP2 may be an efficient approach to control thyroid carcinoma.
Insights
Small interfering RNA (siRNA) targeting retinoblastoma binding protein 2 (RBP2) significantly reduced RBP2 expression in papillary thyroid carcinoma cells. This suppression inhibited cell proliferation, invasion, migration, and tumorigenicity, suggesting RBP2 as a therapeutic target.
Area of Science:
- Molecular Biology
- Oncology
- Gene Regulation
Background:
- Papillary thyroid carcinoma (PTC) is a prevalent endocrine malignancy.
- Retinoblastoma binding protein 2 (RBP2) is implicated in various cancers.
- The role of RBP2 in PTC progression requires further investigation.
Purpose of the Study:
- To investigate the effect of RBP2 knockdown on PTC K1 cell behavior.
- To evaluate RBP2 as a potential therapeutic target in thyroid carcinoma.
Main Methods:
- Transfection of K1 cells with RBP2-specific small interfering RNA (siRNA).
- Assessment of RBP2 mRNA and protein levels via RT-qPCR, Western Blot, and ICC.
- Evaluation of cell proliferation (CCK-8), colony formation (soft agar), invasion, and migration (Transwell assay).
Main Results:
- RBP2-siRNA significantly downregulated RBP2 mRNA and protein expression in K1 cells.
- RBP2 knockdown suppressed cell proliferation, invasion, migration, and tumorigenicity.
- Statistical significance (P<0.01) was observed across multiple assays.
Conclusions:
- Targeting RBP2 with siRNA effectively inhibits key oncogenic properties of papillary thyroid carcinoma cells.
- RBP2 downregulation reduces proliferation, invasion, migration, and tumorigenic potential.
- RBP2 represents a promising molecular target for thyroid carcinoma therapy.
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