fig2

A non-toxic approach for treatment of breast cancer and its metastases: capecitabine enhanced photodynamic therapy in a murine breast tumor model

Figure 2. Physiological and cell death responses to capecitabine pretreatment and photodynamic therapy in murine breast tumor model. Photomicrographs showing 4T1 tumor sections immunohistochemically stained for (A) E-cadherin (E-cad), a marker of differentiation; (B) Ki67, a marker of proliferation, following vehicle or capecitabine (CPBN) treatment; (C) Cell death analysis by terminal-deoxynucleoitidyl transferase dUTP nick end labeling (TUNEL) labeling of apoptotic nuclei at 24 h post photodynamic therapy (PDT), following vehicle or CPBN pre-treatment. Nuclei in images shown in (A-C) were stained with 4’,6-diamidino-2-phenylindole (DAPI); (D) hematoxylin and eosin (H&E) staining of tumor sections showing enhanced cell death at 24 h post PDT in tumors pretreated with CPBN or vehicle alone. Graphs show quantitation of changes in (E) E-cadherin signal; (F) Ki67 signal; and (G) TUNEL positive nuclei per high power field. All graphs show Mean ± SEM from multiple images (number of images shown in parentheses) from three independent experiments. P values from an unpaired two-sided t-test are shown: *P = 1.57 × 10-11; **P = 1.20 × 10-8; ***P = 6.02 × 10-9

Journal of Cancer Metastasis and Treatment
ISSN 2454-2857 (Online) 2394-4722 (Print)

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