Figure 2.
Figure 2. Analysis of a patient-derived xenograft from a KRASG12S-mutant patient with ECD. (A) Fludeoxyglucose positron emission tomography (FDG-PET) imaging and histologic and immunohistochemical analysis of the KRASG12S-mutant ECD patient’s heart biopsy specimen (scale bars represent 200 µm). (B) Flow cytometric analysis of BM, spleen, liver, and lung of recipient NSGS mouse 90 days postxenotransplantation with CD34+ cells from the same KRASG12S-mutant ECD patient. (C) Histologic and immunohistochemical analysis of engrafted tissue from the recipient mouse (scale bars represent 200 µm). (D) Sanger sequencing of genomic DNA from hCD45+ cells purified from recipient mouse BM (left) and spleen (right) revealing a KRASG12S mutation in engrafted human hematopoietic cells. H&E, hematoxylin and eosin.

Analysis of a patient-derived xenograft from a KRASG12S-mutant patient with ECD. (A) Fludeoxyglucose positron emission tomography (FDG-PET) imaging and histologic and immunohistochemical analysis of the KRASG12S-mutant ECD patient’s heart biopsy specimen (scale bars represent 200 µm). (B) Flow cytometric analysis of BM, spleen, liver, and lung of recipient NSGS mouse 90 days postxenotransplantation with CD34+ cells from the same KRASG12S-mutant ECD patient. (C) Histologic and immunohistochemical analysis of engrafted tissue from the recipient mouse (scale bars represent 200 µm). (D) Sanger sequencing of genomic DNA from hCD45+ cells purified from recipient mouse BM (left) and spleen (right) revealing a KRASG12S mutation in engrafted human hematopoietic cells. H&E, hematoxylin and eosin.

Close Modal

or Create an Account

Close Modal
Close Modal