Four-class tumor staging for early diagnosis and monitoring of murine pancreatic cancer using magnetic resonance and ultrasound

E Dugnani, Valentina Pasquale, Paolo Marra, Daniela Liberati, T Canu, L Perani, F De Sanctis, S Ugel, F Invernizzi, A Citro, M Venturini, C Doglioni, A Esposito, L Piemonti

Research output: Contribution to journalArticle

Abstract

Background: The widely used genetically engineered mouse LSL-KrasG12D/+; LSL-Trp53R172H/+; Pdx-1-Cre, termed KPC, spontaneously develops pancreatic cancer mirroring all phases of the carcinogenesis but in asynchronous manner. Preclinical studies need defined criteria for the enrollment of the KPC sharing the same stage of carcinogenesis. Aim: To define a tumor-staging criteria using magnetic resonance (MR) and ultrasound (US) and then to correlate the imaging stage with overall survival of KPC mice. Methods: Forty KPC (2- to 5-month-old mice) were imaged by axial fat-saturated T2-weighted sequences at MR and by brightness mode US to establish criteria for tumor staging. Immunohistopathology was used to validate imaging. A second cohort of 25 KPC was used to correlate imaging stage with survival by Kaplan-Meier analysis. Results: We defined a four-class tumor staging system ranking from stages 1 to 4. Stage 1 was described as radiologically healthy pancreas; precursor lesions were detectable in histology only. Cystic papillary neoplasms, besides other premalignant alterations, marked stage 2 in the absence of cancer nodules. Stages 3 and 4 identified mice affected by overt pancreatic cancer with size
Original languageEnglish
Pages (from-to)1197-1206
Number of pages10
JournalCarcinogenesis
Volume39
Issue number9
DOIs
Publication statusPublished - 2018

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Neoplasm Staging
Pancreatic Neoplasms
Early Diagnosis
Magnetic Resonance Spectroscopy
Carcinogenesis
Kaplan-Meier Estimate
Pancreas
Neoplasms
Histology
Fats

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Four-class tumor staging for early diagnosis and monitoring of murine pancreatic cancer using magnetic resonance and ultrasound. / Dugnani, E; Pasquale, Valentina; Marra, Paolo; Liberati, Daniela; Canu, T; Perani, L; De Sanctis, F; Ugel, S; Invernizzi, F; Citro, A; Venturini, M; Doglioni, C; Esposito, A; Piemonti, L.

In: Carcinogenesis, Vol. 39, No. 9, 2018, p. 1197-1206.

Research output: Contribution to journalArticle

Dugnani, E ; Pasquale, Valentina ; Marra, Paolo ; Liberati, Daniela ; Canu, T ; Perani, L ; De Sanctis, F ; Ugel, S ; Invernizzi, F ; Citro, A ; Venturini, M ; Doglioni, C ; Esposito, A ; Piemonti, L. / Four-class tumor staging for early diagnosis and monitoring of murine pancreatic cancer using magnetic resonance and ultrasound. In: Carcinogenesis. 2018 ; Vol. 39, No. 9. pp. 1197-1206.
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abstract = "Background: The widely used genetically engineered mouse LSL-KrasG12D/+; LSL-Trp53R172H/+; Pdx-1-Cre, termed KPC, spontaneously develops pancreatic cancer mirroring all phases of the carcinogenesis but in asynchronous manner. Preclinical studies need defined criteria for the enrollment of the KPC sharing the same stage of carcinogenesis. Aim: To define a tumor-staging criteria using magnetic resonance (MR) and ultrasound (US) and then to correlate the imaging stage with overall survival of KPC mice. Methods: Forty KPC (2- to 5-month-old mice) were imaged by axial fat-saturated T2-weighted sequences at MR and by brightness mode US to establish criteria for tumor staging. Immunohistopathology was used to validate imaging. A second cohort of 25 KPC was used to correlate imaging stage with survival by Kaplan-Meier analysis. Results: We defined a four-class tumor staging system ranking from stages 1 to 4. Stage 1 was described as radiologically healthy pancreas; precursor lesions were detectable in histology only. Cystic papillary neoplasms, besides other premalignant alterations, marked stage 2 in the absence of cancer nodules. Stages 3 and 4 identified mice affected by overt pancreatic cancer with size",
author = "E Dugnani and Valentina Pasquale and Paolo Marra and Daniela Liberati and T Canu and L Perani and {De Sanctis}, F and S Ugel and F Invernizzi and A Citro and M Venturini and C Doglioni and A Esposito and L Piemonti",
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T1 - Four-class tumor staging for early diagnosis and monitoring of murine pancreatic cancer using magnetic resonance and ultrasound

AU - Dugnani, E

AU - Pasquale, Valentina

AU - Marra, Paolo

AU - Liberati, Daniela

AU - Canu, T

AU - Perani, L

AU - De Sanctis, F

AU - Ugel, S

AU - Invernizzi, F

AU - Citro, A

AU - Venturini, M

AU - Doglioni, C

AU - Esposito, A

AU - Piemonti, L

PY - 2018

Y1 - 2018

N2 - Background: The widely used genetically engineered mouse LSL-KrasG12D/+; LSL-Trp53R172H/+; Pdx-1-Cre, termed KPC, spontaneously develops pancreatic cancer mirroring all phases of the carcinogenesis but in asynchronous manner. Preclinical studies need defined criteria for the enrollment of the KPC sharing the same stage of carcinogenesis. Aim: To define a tumor-staging criteria using magnetic resonance (MR) and ultrasound (US) and then to correlate the imaging stage with overall survival of KPC mice. Methods: Forty KPC (2- to 5-month-old mice) were imaged by axial fat-saturated T2-weighted sequences at MR and by brightness mode US to establish criteria for tumor staging. Immunohistopathology was used to validate imaging. A second cohort of 25 KPC was used to correlate imaging stage with survival by Kaplan-Meier analysis. Results: We defined a four-class tumor staging system ranking from stages 1 to 4. Stage 1 was described as radiologically healthy pancreas; precursor lesions were detectable in histology only. Cystic papillary neoplasms, besides other premalignant alterations, marked stage 2 in the absence of cancer nodules. Stages 3 and 4 identified mice affected by overt pancreatic cancer with size

AB - Background: The widely used genetically engineered mouse LSL-KrasG12D/+; LSL-Trp53R172H/+; Pdx-1-Cre, termed KPC, spontaneously develops pancreatic cancer mirroring all phases of the carcinogenesis but in asynchronous manner. Preclinical studies need defined criteria for the enrollment of the KPC sharing the same stage of carcinogenesis. Aim: To define a tumor-staging criteria using magnetic resonance (MR) and ultrasound (US) and then to correlate the imaging stage with overall survival of KPC mice. Methods: Forty KPC (2- to 5-month-old mice) were imaged by axial fat-saturated T2-weighted sequences at MR and by brightness mode US to establish criteria for tumor staging. Immunohistopathology was used to validate imaging. A second cohort of 25 KPC was used to correlate imaging stage with survival by Kaplan-Meier analysis. Results: We defined a four-class tumor staging system ranking from stages 1 to 4. Stage 1 was described as radiologically healthy pancreas; precursor lesions were detectable in histology only. Cystic papillary neoplasms, besides other premalignant alterations, marked stage 2 in the absence of cancer nodules. Stages 3 and 4 identified mice affected by overt pancreatic cancer with size

U2 - 10.1093/carcin/bgy094

DO - 10.1093/carcin/bgy094

M3 - Article

VL - 39

SP - 1197

EP - 1206

JO - Carcinogenesis

JF - Carcinogenesis

SN - 0143-3334

IS - 9

ER -