Detection and quantitative analysis of early stage orthotopic murine bladder tumor using in vivo magnetic resonance imaging

Eiji Kikuchi, Su Xu, Makoto Ohori, Cornelia Matei, Mihaela Lupu, Silvia Menendez, Jason A. Koutcher, Bernard H. Bochner

Research output: Contribution to journalArticle

23 Citations (Scopus)

Abstract

Purpose: We evaluated in vivo magnetic resonance imaging (MRI) as a noninvasive method for early detection and quantitative measurements of superficial tumors in an orthotopic murine bladder tumor model. Materials and Methods: Murine bladder tumor cells were instilled into 25 mouse bladders and subsequently scanned with MRI 10, 14, 17 and 24 days after tumor inoculation. High quality T1-weighted spin-echo transverse images were obtained with 1.5 mm thick slices. Conditions for contrast agent instillation were optimized by evaluating varying concentrations of Gd-diethylenetetramine pentaacetic acid, water and air. Total tumor area in the largest bladder section on MRI was measured and compared quantitatively with actual tumor areas measured in whole mount bladder step sections. Results: Optimal MRI studies were obtained with intravesical instillation of 50 μl Gd-diethylenetetramine pentaacetic acid and 50 μl air. Overall 17 tumors in 11 mice were identified pathologically 10 days after tumor inoculation, of which 14 (82.4%) were identified by MRI with a largest mean diameter of 1.4 ± 0.1 mm (range 1.0 to 2.2). Mean total tumor area on MRI 10, 14, 17 and 24 days after tumor inoculation was 0. 024 ± 0.005, 0.108 ± 0.049, 0.165 ± 0.020 and 0.318 ± 0.023 cm2, respectively, which correlated well with actual tumor area (r2 = 0.977, p <0.001). Conclusions: MRI is accurate and effective for noninvasively monitoring tumor growth in the orthotopic murine bladder cancer model. The improved resolution that we report compared with previous murine bladder studies highlights its potential for monitoring the therapeutic efficacy of antitumor agents for early superficial bladder tumors.

Original languageEnglish
Pages (from-to)1375-1378
Number of pages4
JournalJournal of Urology
Volume170
Issue number4 I
DOIs
Publication statusPublished - 2003 Oct 1
Externally publishedYes

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Urinary Bladder Neoplasms
Magnetic Resonance Imaging
Neoplasms
Urinary Bladder
Air
Intravesical Administration
Acids
Antineoplastic Agents
Contrast Media
Water
Growth

Keywords

  • Bladder
  • Bladder neoplasms
  • Magnetic resonance imaging
  • Mice

ASJC Scopus subject areas

  • Urology

Cite this

Detection and quantitative analysis of early stage orthotopic murine bladder tumor using in vivo magnetic resonance imaging. / Kikuchi, Eiji; Xu, Su; Ohori, Makoto; Matei, Cornelia; Lupu, Mihaela; Menendez, Silvia; Koutcher, Jason A.; Bochner, Bernard H.

In: Journal of Urology, Vol. 170, No. 4 I, 01.10.2003, p. 1375-1378.

Research output: Contribution to journalArticle

Kikuchi, E, Xu, S, Ohori, M, Matei, C, Lupu, M, Menendez, S, Koutcher, JA & Bochner, BH 2003, 'Detection and quantitative analysis of early stage orthotopic murine bladder tumor using in vivo magnetic resonance imaging', Journal of Urology, vol. 170, no. 4 I, pp. 1375-1378. https://doi.org/10.1097/01.ju.0000075504.13456.41
Kikuchi, Eiji ; Xu, Su ; Ohori, Makoto ; Matei, Cornelia ; Lupu, Mihaela ; Menendez, Silvia ; Koutcher, Jason A. ; Bochner, Bernard H. / Detection and quantitative analysis of early stage orthotopic murine bladder tumor using in vivo magnetic resonance imaging. In: Journal of Urology. 2003 ; Vol. 170, No. 4 I. pp. 1375-1378.
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AU - Kikuchi, Eiji

AU - Xu, Su

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AU - Lupu, Mihaela

AU - Menendez, Silvia

AU - Koutcher, Jason A.

AU - Bochner, Bernard H.

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N2 - Purpose: We evaluated in vivo magnetic resonance imaging (MRI) as a noninvasive method for early detection and quantitative measurements of superficial tumors in an orthotopic murine bladder tumor model. Materials and Methods: Murine bladder tumor cells were instilled into 25 mouse bladders and subsequently scanned with MRI 10, 14, 17 and 24 days after tumor inoculation. High quality T1-weighted spin-echo transverse images were obtained with 1.5 mm thick slices. Conditions for contrast agent instillation were optimized by evaluating varying concentrations of Gd-diethylenetetramine pentaacetic acid, water and air. Total tumor area in the largest bladder section on MRI was measured and compared quantitatively with actual tumor areas measured in whole mount bladder step sections. Results: Optimal MRI studies were obtained with intravesical instillation of 50 μl Gd-diethylenetetramine pentaacetic acid and 50 μl air. Overall 17 tumors in 11 mice were identified pathologically 10 days after tumor inoculation, of which 14 (82.4%) were identified by MRI with a largest mean diameter of 1.4 ± 0.1 mm (range 1.0 to 2.2). Mean total tumor area on MRI 10, 14, 17 and 24 days after tumor inoculation was 0. 024 ± 0.005, 0.108 ± 0.049, 0.165 ± 0.020 and 0.318 ± 0.023 cm2, respectively, which correlated well with actual tumor area (r2 = 0.977, p <0.001). Conclusions: MRI is accurate and effective for noninvasively monitoring tumor growth in the orthotopic murine bladder cancer model. The improved resolution that we report compared with previous murine bladder studies highlights its potential for monitoring the therapeutic efficacy of antitumor agents for early superficial bladder tumors.

AB - Purpose: We evaluated in vivo magnetic resonance imaging (MRI) as a noninvasive method for early detection and quantitative measurements of superficial tumors in an orthotopic murine bladder tumor model. Materials and Methods: Murine bladder tumor cells were instilled into 25 mouse bladders and subsequently scanned with MRI 10, 14, 17 and 24 days after tumor inoculation. High quality T1-weighted spin-echo transverse images were obtained with 1.5 mm thick slices. Conditions for contrast agent instillation were optimized by evaluating varying concentrations of Gd-diethylenetetramine pentaacetic acid, water and air. Total tumor area in the largest bladder section on MRI was measured and compared quantitatively with actual tumor areas measured in whole mount bladder step sections. Results: Optimal MRI studies were obtained with intravesical instillation of 50 μl Gd-diethylenetetramine pentaacetic acid and 50 μl air. Overall 17 tumors in 11 mice were identified pathologically 10 days after tumor inoculation, of which 14 (82.4%) were identified by MRI with a largest mean diameter of 1.4 ± 0.1 mm (range 1.0 to 2.2). Mean total tumor area on MRI 10, 14, 17 and 24 days after tumor inoculation was 0. 024 ± 0.005, 0.108 ± 0.049, 0.165 ± 0.020 and 0.318 ± 0.023 cm2, respectively, which correlated well with actual tumor area (r2 = 0.977, p <0.001). Conclusions: MRI is accurate and effective for noninvasively monitoring tumor growth in the orthotopic murine bladder cancer model. The improved resolution that we report compared with previous murine bladder studies highlights its potential for monitoring the therapeutic efficacy of antitumor agents for early superficial bladder tumors.

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