Cargando…

Investigation of breast cancer microstructure and microvasculature from time-dependent DWI and CEST in correlation with histological biomarkers

We investigated the associations of time-dependent DWI, non-Gaussian DWI, and CEST parameters with histological biomarkers in a breast cancer xenograft model. 22 xenograft mice (7 MCF-7 and 15 MDA-MB-231) were scanned at 4 diffusion times [T(d) = 2.5/5 ms with 11 b-values (0–600 s/mm(2)) and T(d) = ...

Descripción completa

Detalles Bibliográficos
Autores principales: Someya, Yuko, Iima, Mami, Imai, Hirohiko, Yoshizawa, Akihiko, Kataoka, Masako, Isoda, Hiroyoshi, Le Bihan, Denis, Nakamoto, Yuji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9021220/
https://www.ncbi.nlm.nih.gov/pubmed/35444193
http://dx.doi.org/10.1038/s41598-022-10081-7
_version_ 1784689758948032512
author Someya, Yuko
Iima, Mami
Imai, Hirohiko
Yoshizawa, Akihiko
Kataoka, Masako
Isoda, Hiroyoshi
Le Bihan, Denis
Nakamoto, Yuji
author_facet Someya, Yuko
Iima, Mami
Imai, Hirohiko
Yoshizawa, Akihiko
Kataoka, Masako
Isoda, Hiroyoshi
Le Bihan, Denis
Nakamoto, Yuji
author_sort Someya, Yuko
collection PubMed
description We investigated the associations of time-dependent DWI, non-Gaussian DWI, and CEST parameters with histological biomarkers in a breast cancer xenograft model. 22 xenograft mice (7 MCF-7 and 15 MDA-MB-231) were scanned at 4 diffusion times [T(d) = 2.5/5 ms with 11 b-values (0–600 s/mm(2)) and T(d) = 9/27.6 ms with 17 b-values (0–3000 s/mm(2)), respectively]. The apparent diffusion coefficient (ADC) was estimated using 2 b-values in different combinations (ADC(0–600) using b = 0 and 600 s/mm(2) and shifted ADC [sADC(200–1500)] using b = 200 and 1500 s/mm(2)) at each of those diffusion times. Then the change (Δ) in ADC/sADC between diffusion times was evaluated. Non-Gaussian diffusion and intravoxel incoherent motion (IVIM) parameters (ADC(0), the virtual ADC at b = 0; K, Kurtosis from non-Gaussian diffusion; f, the IVIM perfusion fraction) were estimated. CEST images were acquired and the amide proton transfer signal intensity (APT SI) were measured. The ΔsADC(9–27.6) (between [Formula: see text] and [Formula: see text] and ΔADC(2.5)_sADC(27.6) (between [Formula: see text] and [Formula: see text] ) was significantly larger for MCF-7 groups, and ΔADC(2.5)_sADC(27.6) was positively correlated with Ki67(max) and APT SI. ADC(0) decreased significantly in MDA-MB-231 group and K increased significantly with T(d) in MCF-7 group. APT SI and cellular area had a moderately strong positive correlation in MDA-MB-231 and MCF-7 tumors combined, and there was a positive correlation in MDA-MB-231 tumors. There was a significant negative correlation between APT SI and the Ki-67-positive ratio in MDA-MB-231 tumors and when combined with MCF-7 tumors. The associations of ΔADC(2.5)_sADC(27.6) and API SI with Ki-67 parameters indicate that the T(d)-dependent DW and CEST parameters are useful to predict the histological markers of breast cancers.
format Online
Article
Text
id pubmed-9021220
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-90212202022-04-21 Investigation of breast cancer microstructure and microvasculature from time-dependent DWI and CEST in correlation with histological biomarkers Someya, Yuko Iima, Mami Imai, Hirohiko Yoshizawa, Akihiko Kataoka, Masako Isoda, Hiroyoshi Le Bihan, Denis Nakamoto, Yuji Sci Rep Article We investigated the associations of time-dependent DWI, non-Gaussian DWI, and CEST parameters with histological biomarkers in a breast cancer xenograft model. 22 xenograft mice (7 MCF-7 and 15 MDA-MB-231) were scanned at 4 diffusion times [T(d) = 2.5/5 ms with 11 b-values (0–600 s/mm(2)) and T(d) = 9/27.6 ms with 17 b-values (0–3000 s/mm(2)), respectively]. The apparent diffusion coefficient (ADC) was estimated using 2 b-values in different combinations (ADC(0–600) using b = 0 and 600 s/mm(2) and shifted ADC [sADC(200–1500)] using b = 200 and 1500 s/mm(2)) at each of those diffusion times. Then the change (Δ) in ADC/sADC between diffusion times was evaluated. Non-Gaussian diffusion and intravoxel incoherent motion (IVIM) parameters (ADC(0), the virtual ADC at b = 0; K, Kurtosis from non-Gaussian diffusion; f, the IVIM perfusion fraction) were estimated. CEST images were acquired and the amide proton transfer signal intensity (APT SI) were measured. The ΔsADC(9–27.6) (between [Formula: see text] and [Formula: see text] and ΔADC(2.5)_sADC(27.6) (between [Formula: see text] and [Formula: see text] ) was significantly larger for MCF-7 groups, and ΔADC(2.5)_sADC(27.6) was positively correlated with Ki67(max) and APT SI. ADC(0) decreased significantly in MDA-MB-231 group and K increased significantly with T(d) in MCF-7 group. APT SI and cellular area had a moderately strong positive correlation in MDA-MB-231 and MCF-7 tumors combined, and there was a positive correlation in MDA-MB-231 tumors. There was a significant negative correlation between APT SI and the Ki-67-positive ratio in MDA-MB-231 tumors and when combined with MCF-7 tumors. The associations of ΔADC(2.5)_sADC(27.6) and API SI with Ki-67 parameters indicate that the T(d)-dependent DW and CEST parameters are useful to predict the histological markers of breast cancers. Nature Publishing Group UK 2022-04-20 /pmc/articles/PMC9021220/ /pubmed/35444193 http://dx.doi.org/10.1038/s41598-022-10081-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Someya, Yuko
Iima, Mami
Imai, Hirohiko
Yoshizawa, Akihiko
Kataoka, Masako
Isoda, Hiroyoshi
Le Bihan, Denis
Nakamoto, Yuji
Investigation of breast cancer microstructure and microvasculature from time-dependent DWI and CEST in correlation with histological biomarkers
title Investigation of breast cancer microstructure and microvasculature from time-dependent DWI and CEST in correlation with histological biomarkers
title_full Investigation of breast cancer microstructure and microvasculature from time-dependent DWI and CEST in correlation with histological biomarkers
title_fullStr Investigation of breast cancer microstructure and microvasculature from time-dependent DWI and CEST in correlation with histological biomarkers
title_full_unstemmed Investigation of breast cancer microstructure and microvasculature from time-dependent DWI and CEST in correlation with histological biomarkers
title_short Investigation of breast cancer microstructure and microvasculature from time-dependent DWI and CEST in correlation with histological biomarkers
title_sort investigation of breast cancer microstructure and microvasculature from time-dependent dwi and cest in correlation with histological biomarkers
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9021220/
https://www.ncbi.nlm.nih.gov/pubmed/35444193
http://dx.doi.org/10.1038/s41598-022-10081-7
work_keys_str_mv AT someyayuko investigationofbreastcancermicrostructureandmicrovasculaturefromtimedependentdwiandcestincorrelationwithhistologicalbiomarkers
AT iimamami investigationofbreastcancermicrostructureandmicrovasculaturefromtimedependentdwiandcestincorrelationwithhistologicalbiomarkers
AT imaihirohiko investigationofbreastcancermicrostructureandmicrovasculaturefromtimedependentdwiandcestincorrelationwithhistologicalbiomarkers
AT yoshizawaakihiko investigationofbreastcancermicrostructureandmicrovasculaturefromtimedependentdwiandcestincorrelationwithhistologicalbiomarkers
AT kataokamasako investigationofbreastcancermicrostructureandmicrovasculaturefromtimedependentdwiandcestincorrelationwithhistologicalbiomarkers
AT isodahiroyoshi investigationofbreastcancermicrostructureandmicrovasculaturefromtimedependentdwiandcestincorrelationwithhistologicalbiomarkers
AT lebihandenis investigationofbreastcancermicrostructureandmicrovasculaturefromtimedependentdwiandcestincorrelationwithhistologicalbiomarkers
AT nakamotoyuji investigationofbreastcancermicrostructureandmicrovasculaturefromtimedependentdwiandcestincorrelationwithhistologicalbiomarkers