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Cellular senescence is associated with the spatial evolution toward a higher metastatic phenotype in colorectal cancer

In this study, we explore the dynamic process of colorectal cancer progression, emphasizing the evolution toward a more metastatic phenotype. The term “evolution” as used in this study specifically denotes the phenotypic transition toward a higher metastatic potency from well-formed glandular struct...

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Published in:Cell reports (Cambridge) 2024-03, Vol.43 (3), p.113912-113912, Article 113912
Main Authors: Park, Soon Sang, Lee, Young-Kyoung, Choi, Yong Won, Lim, Su Bin, Park, So Hyun, Kim, Han Ki, Shin, Jun Sang, Kim, Young Hwa, Lee, Dong Hyun, Kim, Jang-Hee, Park, Tae Jun
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cited_by cdi_FETCH-LOGICAL-c474t-896e8ac2c6c357b5cdb2523b28a7147c90920ab117b3637e57db1080608f6df3
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container_title Cell reports (Cambridge)
container_volume 43
creator Park, Soon Sang
Lee, Young-Kyoung
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Lim, Su Bin
Park, So Hyun
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Shin, Jun Sang
Kim, Young Hwa
Lee, Dong Hyun
Kim, Jang-Hee
Park, Tae Jun
description In this study, we explore the dynamic process of colorectal cancer progression, emphasizing the evolution toward a more metastatic phenotype. The term “evolution” as used in this study specifically denotes the phenotypic transition toward a higher metastatic potency from well-formed glandular structures to collective invasion, ultimately resulting in the development of cancer cell buddings at the invasive front. Our findings highlight the spatial correlation of this evolution with tumor cell senescence, revealing distinct types of senescent tumor cells (types I and II) that play different roles in the overall cancer progression. Type I senescent tumor cells (p16INK4A+/CXCL12+/LAMC2−/MMP7−) are identified in the collective invasion region, whereas type II senescent tumor cells (p16INK4A+/CXCL12+/LAMC2+/MMP7+), representing the final evolved form, are prominently located in the partial-EMT region. Importantly, type II senescent tumor cells associate with local invasion and lymph node metastasis in colorectal cancer, potentially affecting patient prognosis. [Display omitted] •Cellular senescence is associated with gradual phenotypic transition of cancer cells•Evolutionary path of cancer cells includes two types (I and II) of senescent tumor cells•Type II senescent tumor cells express MMP7 and are associated with higher metastatic potency Park et al. unravel the spatial heterogeneity of colorectal cancer and gradual phenotypic transition from the center to the invasive front. They demonstrated that cellular senescence is associated with this evolutional transition. Type II senescent tumor cells (p16INK4A+/LAMC2+/MMP7+) were found in the invasive front and are associated with higher metastatic potency.
doi_str_mv 10.1016/j.celrep.2024.113912
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The term “evolution” as used in this study specifically denotes the phenotypic transition toward a higher metastatic potency from well-formed glandular structures to collective invasion, ultimately resulting in the development of cancer cell buddings at the invasive front. Our findings highlight the spatial correlation of this evolution with tumor cell senescence, revealing distinct types of senescent tumor cells (types I and II) that play different roles in the overall cancer progression. Type I senescent tumor cells (p16INK4A+/CXCL12+/LAMC2−/MMP7−) are identified in the collective invasion region, whereas type II senescent tumor cells (p16INK4A+/CXCL12+/LAMC2+/MMP7+), representing the final evolved form, are prominently located in the partial-EMT region. Importantly, type II senescent tumor cells associate with local invasion and lymph node metastasis in colorectal cancer, potentially affecting patient prognosis. [Display omitted] •Cellular senescence is associated with gradual phenotypic transition of cancer cells•Evolutionary path of cancer cells includes two types (I and II) of senescent tumor cells•Type II senescent tumor cells express MMP7 and are associated with higher metastatic potency Park et al. unravel the spatial heterogeneity of colorectal cancer and gradual phenotypic transition from the center to the invasive front. They demonstrated that cellular senescence is associated with this evolutional transition. 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subjects cancer buddings
cancer evolution
Cellular Senescence - genetics
collective invasion
colorectal cancer
Colorectal Neoplasms - genetics
Colorectal Neoplasms - pathology
CP: Cancer
Cyclin-Dependent Kinase Inhibitor p16 - metabolism
Humans
LAMC2
lymph node metastasis
Matrix Metalloproteinase 7 - genetics
MMP7
Phenotype
senescent tumor cells
spatial evolution
spatial transcriptomics
title Cellular senescence is associated with the spatial evolution toward a higher metastatic phenotype in colorectal cancer
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