Detail of Fig1C_organoid_AKTP

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Project
Title
HS-SICM topographic images of the apical surface of the cells of the ApcDelta716 KrasG12D Tgfbr2-/- Trp53R270H tumor-derived organoids (AKTP).
Description
HS-SICM topographic images of the apical surface of the cells of the ApcDelta716 KrasG12D Tgfbr2-/- Trp53R270H tumor-derived organoids (AKTP).
Release, Updated
2023-07-20
License
CC BY
Kind
Image data
File Formats
.png
Data size
469.3 KB

Organism
Mus musculus ( NCBI:txid10090 )
Strain(s)
C57BL/6
Cell Line
-

Datatype
-
Molecular Function (MF)
Biological Process (BP)
Cellular Component (CC)
cell surface ( GO:0009986 )
Biological Imaging Method
high-speed (HS)-scanning ion conductance microscopy
X scale
2 micrometer/pixel
Y scale
2 micrometer/pixel
Z scale
-
T scale
-

Image Acquisition
Experiment type
-
Microscope type
-
Acquisition mode
-
Contrast method
-
Microscope model
-
Detector model
-
Objective model
-
Filter set
-

Summary of Methods
See details in Wang D, et. al. (2022) Biomaterials, Jan;280:121256.
Related paper(s)

Dong Wang, Linhao Sun, Satoru Okuda, Daisuke Yamamoto, Mizuho Nakayama, Hiroko Oshima, Hideyuki Saito, Yuta Kouyama, Koshi Mimori, Toshio Ando, Shinji Watanabe, Masanobu Oshima (2022) Nano-scale physical properties characteristic to metastatic intestinal cancer cells identified by high-speed scanning ion conductance microscope., Biomaterials, Volume 280, pp. 121256

Published in 2022 Jan (Electronic publication in Nov. 13, 2021, midnight )

(Abstract) Recent genetic studies have indicated relationships between gene mutations and colon cancer phenotypes. However, how physical properties of tumor cells are changed by genetic alterations has not been elucidated. We examined genotype-defined mouse intestinal tumor-derived cells using a high-speed scanning ion conductance microscope (HS-SICM) that can obtain high-resolution live images of nano-scale topography and stiffness. The tumor cells used in this study carried mutations in Apc (A), Kras (K), Tgfbr2 (T), Trp53 (P), and Fbxw7 (F) in various combinations. Notably, high-metastatic cancer-derived cells carrying AKT mutations (AKT, AKTP, and AKTPF) showed specific ridge-like morphology with active membrane volume change, which was not found in low-metastatic and adenoma-derived cells. Furthermore, the membrane was significantly softer in the metastatic AKT-type cancer cells than other genotype cells. Importantly, a principal component analysis using RNAseq data showed similar distributions of expression profiles and physical properties, indicating a link between genetic alterations and physical properties. Finally, the malignant cell-specific physical properties were confirmed by an HS-SICM using human colon cancer-derived cells. These results indicate that the HS-SICM analysis is useful as a novel diagnostic strategy for predicting the metastatic ability of cancer cells.
(MeSH Terms)

Contact
Masanobu Oshima , Kanazawa University , Cancer Research Institute , WPI Nano-Life Science Institute
Contributors

OMERO Dataset
OMERO Project
Source