[Corrigendum] Characteristics of myeloid sarcoma in mice and patients with TET2 deficiency
Affiliations: Department of Oncology, Second Hospital of Tianjin Medical University, Tianjin 300211, P.R. China, Department of Hematology, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin's Clinical Research Center for Cancer, Tianjin 300060, P.R. China, Department of Hematology, The Union Hospital of Tongji Medical College of Huazhong University of Science and Technology, Wuhan, Hubei 430030, P.R. China, Department of Hematology, The First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, P.R. China, Sylvester Comprehensive Cancer Center, Department of Biochemistry and Molecular Biology, University of Miami Miller School of Medicine, Miami, FL 33136, USA
- Published online on: July 24, 2020 https://doi.org/10.3892/ol.2020.11907
- Article Number: 41
Copyright : © Wang et al. This is an open access article distributed under the terms of Creative Commons Attribution License [CC BY 4.0].
This article is mentioned in:
Oncol Lett 19: [Related article:] 3789-3798, 2020; DOI: 10.3892/ol.2020.11479
Subsequently to the publication of the above article, the authors have realized that three of the four fluorescence-activated cell sorting (FACS) images in Fig. 2B were selected incorrectly. Furthermore, the pie charts shown in Fig. 3A were labelled incorrectly; essentially, the pie charts from left to right should have been labelled as ‘Myeloid malignancy’ and ‘Normal’, respectively).
Sarcoma cells in TET2−/− mice are transplantable. (A) Tumor transfer schema. Sarcoma cells (1x106) from a representative TET2−/− mouse with MS or BM cells (1x106) from an age-matched WT mouse were injected into sub-lethally irradiated (800 cGy) recipients (n=5). (B) Flow cytometric analyses of periph- eral blood myeloid lineage (Mac1+/Gr1+) donor cells (CD45.2+) from a mouse receiving BM cells from a WT mouse or sarcoma cells from a TET2−/− mouse with MS mass. (C) Hematoxylin and eosin-stained histological sections of spleen and liver from a representative recipient mouse. Infiltration of a uniform myeloid malignancy cell population was identified in spleen and liver. Infiltrating patterns and cell morphology were similar to those observed in the donor (MS) mouse. These data demonstrate that the recipients receiving MS cells developed a disease similar to their donor mouse. Magnification, x200. (D) Most of the recipients exhibited elevated WBC monocyte, and decreased RBC counts (n=5). (E) Kaplan-Meier survival curve of sub-lethally irradiated recipients transplanted with BM cells (1x106) from a WT mouse or MS cells from TET2−/− mice. WT, wild-type; MS, myeloid sarcoma; BM, bone marrow.
Salvage effect of 5-Aza-dC for TET2−/− myeloid malignancies. (A) Proportions of myeloid malignancies in mice of 5-Aza-dC treated TET2−/− cohorts were lower after half-a-year of (A) follow-up with (B) an improved survival. (C) Weight of spleen from representative TET2−/− mice and TET2−/− mice treated with 5-Aza-dC, as well as age-matched WT mice. (D) Photos of spleen from representative TET2−/− mice and TET2−/− mice with 5-Aza-dC treatment, as well as age-matched WT mice. WT, wild-type.
Corrected versions of Figs. 2 and 3 are shown on the next page. The authors would like to thank the Editor of Oncology Letters for allowing them the opportunity to publish this corrigendum, and apologize to the readership of the Journal for any inconvenience caused.