Abstract
In the published article, there was an error in Figure 3, panel J as published. We inadvertently used the incorrect image for the RCM1-NPFA IVIS image on Day 9 in panel 3J. The corrected Figure 3 and its caption appear below. Generation of nanoparticle to deliver RCM1 to tumors. (A), Graphic of amphiphilic poly-beta amino ester (aPBAE) nanoparticles without folic acid (NP, top) and with folic acid (NPFA, bottom). (B), Highly efficient delivery of NPFA, compared to NP into the tumors is shown using IVIS imaging. Mice bearing Rd76-9 subcutaneous RMS tumors were injected with NP or NPFA labeled with DyLight 800. NPFA are present in the tumor 48 hours after i.v. injection. (C), Average radiant efficiency indicating NPFA have a higher intensity compared to NP. (D), The sizes of NPFA were measured and the hydrodynamic average diameter of NPFA is 160.67nm. (E), The surface charge of NPFA is 38.13mV. (F), The UV/Vis spectrum for RCM1 at increasing concentrations in DMSO determined RCM1 has an absorbance peak at 310nm and 395nm. (G), Data from the UV/VIS spectra was used to generate a standard concentration curve that was used to determine RCM1 concentration in the nanoparticles. Adjusted R2 = 0.99944. (H), Schematic diagram showing treatment strategy of tumor bearing mice. Rhabdomyosarcoma Rd76-9 cells were inoculated subcutaneously. Animals were treated with 4µg, 8µg, or 16µg RCM1- NPFA. (I), Treatment with RCM1-NPFA reduced tumor burden in a dose-dependent manner in animals. Mice were treated with 4µg, 8µg, or 16µg of RCM1-NPFA or with empty-NPFA. Tumor volumes were measured at different time points compared to empty-NPFA (top panel). Representative tumors per group are shown (bottom panel). Values are shown as mean ± SD. n=3-7, *P<0.05; ***P<0.001. (J), Presence of Empty-NPFA and RCM1-NPFA nanoparticles in the tumors are shown at days 9 and 15 after treatment. Nanoparticles were labeled with DyLight 800 and visualized using IVIS. The authors apologize for this error and state that this does not change the scientific conclusions of the article in any way. The original article has been updated.
| Original language | English (US) |
|---|---|
| Article number | 1163510 |
| Journal | Frontiers in Oncology |
| Volume | 13 |
| DOIs |
|
| State | Published - 2023 |
| Externally published | Yes |
Keywords
- FOXM1 inhibitor
- animal models
- combination therapy
- nanoparticles
- rhabdomyosarcoma
ASJC Scopus subject areas
- Oncology
- Cancer Research
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Dive into the research topics of 'Corrigendum: Improving anti-tumor efficacy of low-dose Vincristine in rhabdomyosarcoma via the combination therapy with FOXM1 inhibitor RCM1 (Frontiers in Oncology, (2023), 13, (1112859), 10.3389/fonc.2023.1112859)'. Together they form a unique fingerprint.Cite this
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