Raphical illustration of the longterm luciferase expression from NOD-SCID mice injected with either Huh7 or MIA-PaCa2 stable cell lines (n = 3 for Huh7 and n = 4 for MIA-PaCa2). Luciferase quantitation is expressed, as photons/sec/cm2/sr and plotted (+/2 SD). Background level of light emission on non-treated animals is 56105 photons/sec/cm2/sr. doi:10.1371/journal.pone.0047920.gHistological Analysis of the Formed TumoursHaematoxylin and eosin stained tissue sections were performed to identify LY-2409021 site tumour histology derived from each cell line. Figure 3 shows histology sections of tumours formed from Huh7 cells. Histology Methyl linolenate site confirms that the tumour is a hepatocellular carcinoma (HCC) with varying degrees of differentiation (Figure 3A ). The tumour is composed of polygonal cells distributed in loose sheets and pseudoglandular patterns. The nuclei were moderately pleomorphic, vesicular and contain a nucleolus. A few isolated mitotic figures were also noted. The cytoplasm was eosinophilic and the cell borders were well defined, while the stroma was scanty. Intracellular and extracellular bile droplets were not seen in the tumour and neither was tumour necrosis. The features of the tumour were confirmed by an independent histopathologist tobe consistent with a Grade II HCC (modified Edmonson and Steiner’s grading system). In addition luciferase 25033180 immunohistochemical analysis of tumour sections (Figure 3B and 3C) showed all hepatocyte-like cells derived from the injected cells to be expressing luciferase. Unstained areas are believed to be either necrotic tissue or cells recruited to the tumour, which has not yet been confirmed experimentally and is currently under investigation. Similarly, haemotoxylin and eosin stained tissue sections were obtained for the tumours formed in mice after injection of MIAPaCa2 cells (Figure 3E ). In this case, the histological sections revealed that the formed tumour cells had permeated between the normal pancreatic acini at the periphery of the tumour. The tumour cells were described to be distributed in solid sheets with no evidence of glandular differentiation and have a moderate amount of cytoplasm with well-defined cell borders. The nucleiS/MAR Vectors for In Vivo Tumour ModellingFigure 3. Histochemistry and Immunohistochemistry of tumour sections at day 35 post delivery, showing the formation of a hepatocellular carcinoma-like tumour and a pancreatic carcinoma tumour, to which luciferase expression localises. Sections from different parts of the two tumours were cut and stained with haematoxylin and eosin for histological analysis of the tumours. A ) Sections from Huh7 injected mice. Sections have an amorphous structure and were identified as hepatocellular carcinoma (HCC) of varying degrees of differentiation: (A) Moderately differentiated HCC, magnification610 (B ) Sections were analysed by immunohistochemistry to show distribution of luciferase expression. Brown staining indicates luciferase positive cells. (B) Positively stained, Magnification640 (C) Positively stained, Magnification610 (D) Negative control: no primary antibody added, magnification610 E ) Sections from MIA-PaCa2 injected mice. Sections have an amorphous structure and were identified as Pancreatic carcinoma (PaCa) of varying degrees of differentiation. (E) Moderately differentiated PaCa, magnification610 (F ) Sections were analysed by immunohistochemistry 
to show distribution of luciferase expression. Brown staining indicates luciferase positive.Raphical illustration of the longterm luciferase expression from NOD-SCID mice injected with either Huh7 or MIA-PaCa2 stable cell lines (n = 3 for Huh7 and n = 4 for MIA-PaCa2). Luciferase quantitation is expressed, as photons/sec/cm2/sr and plotted (+/2 SD). Background level of light emission on non-treated animals is 56105 photons/sec/cm2/sr. doi:10.1371/journal.pone.0047920.gHistological Analysis of the Formed TumoursHaematoxylin and eosin stained tissue sections were performed to identify tumour histology derived from each cell line. Figure 3 shows histology sections of tumours formed from Huh7 cells. Histology confirms that the tumour is a hepatocellular carcinoma (HCC) with varying degrees of differentiation (Figure 3A ). The tumour is composed of polygonal cells distributed in loose sheets and pseudoglandular patterns. The nuclei were moderately pleomorphic, vesicular and contain a nucleolus. A few isolated mitotic figures were also noted. The cytoplasm was eosinophilic and the cell borders were well defined, while the stroma was scanty. Intracellular and extracellular bile droplets were not seen in the tumour and neither was tumour necrosis. The features of the tumour were confirmed by an independent histopathologist tobe consistent with a Grade II HCC (modified Edmonson and Steiner’s grading system). In addition luciferase 25033180 immunohistochemical analysis of tumour sections (Figure 3B and 3C) showed all hepatocyte-like cells derived from the injected cells to be expressing luciferase. Unstained areas are believed to be either necrotic tissue or cells recruited to the tumour, which has not yet been confirmed experimentally and is currently under investigation. Similarly, haemotoxylin and eosin stained tissue sections were obtained for the tumours formed in mice after injection of MIAPaCa2 cells (Figure 3E ). In this case, the histological sections revealed that the formed tumour cells had permeated between the normal pancreatic acini at the periphery of the tumour. The tumour cells were described to be distributed in solid sheets with no evidence of glandular differentiation and have a moderate amount of cytoplasm with well-defined cell borders. The nucleiS/MAR Vectors for In Vivo Tumour ModellingFigure 3. Histochemistry and Immunohistochemistry of tumour sections at day 35 post delivery, showing the formation of a hepatocellular carcinoma-like tumour and a pancreatic carcinoma tumour, to which luciferase expression localises. Sections from different parts of the two tumours were cut and stained with haematoxylin and eosin for histological analysis of the tumours. A ) Sections from Huh7 injected mice. Sections 
have an amorphous structure and were identified as hepatocellular carcinoma (HCC) of varying degrees of differentiation: (A) Moderately differentiated HCC, magnification610 (B ) Sections were analysed by immunohistochemistry to show distribution of luciferase expression. Brown staining indicates luciferase positive cells. (B) Positively stained, Magnification640 (C) Positively stained, Magnification610 (D) Negative control: no primary antibody added, magnification610 E ) Sections from MIA-PaCa2 injected mice. Sections have an amorphous structure and were identified as Pancreatic carcinoma (PaCa) of varying degrees of differentiation. (E) Moderately differentiated PaCa, magnification610 (F ) Sections were analysed by immunohistochemistry to show distribution of luciferase expression. Brown staining indicates luciferase positive.
