Establishing a Highly Accurate Circulating Tumor Cell Image Recognition System for Human Lung Cancer by Pre-Training on Lung Cancer Cell Lines

Background/Objectives: Circulating tumor cells (CTCs) are important biomarkers for predicting prognosis and evaluating treatment efficacy in cancer. We developed the “CTC-Chip” system based on microfluidics, enabling highly sensitive CTC detection and prognostic assessment in lung cancer and maligna...

Full description

Saved in:
Bibliographic Details
Published inCancers Vol. 17; no. 14; p. 2289
Main Authors Matsumiya, Hiroki, Terabayashi, Kenji, Kishi, Yusuke, Yoshino, Yuki, Mori, Masataka, Kanayama, Masatoshi, Oyama, Rintaro, Nemoto, Yukiko, Nishizawa, Natsumasa, Honda, Yohei, Kuwata, Taiji, Takenaka, Masaru, Chikaishi, Yasuhiro, Yoneda, Kazue, Kuroda, Koji, Ohnaga, Takashi, Sasaki, Tohru, Tanaka, Fumihiro
Format Journal Article
LanguageEnglish
Published Switzerland MDPI AG 09.07.2025
MDPI
Subjects
Online AccessGet full text
ISSN2072-6694
2072-6694
DOI10.3390/cancers17142289

Cover

Abstract Background/Objectives: Circulating tumor cells (CTCs) are important biomarkers for predicting prognosis and evaluating treatment efficacy in cancer. We developed the “CTC-Chip” system based on microfluidics, enabling highly sensitive CTC detection and prognostic assessment in lung cancer and malignant pleural mesothelioma. However, the final identification and enumeration of CTCs require manual intervention, which is time-consuming, prone to human error, and necessitates the involvement of experienced medical professionals. Medical image recognition using machine learning can reduce workload and improve automation. However, CTCs are rare in clinical samples, limiting the training data available to construct a robust CTC image recognition system. In this study, we established a highly accurate artificial intelligence-based CTC recognition system by pre-training convolutional neural networks using images from lung cancer cell lines. Methods: We performed transfer learning of convolutional neural networks. Initially, the models were pre-trained using images obtained from lung cancer cell lines. The model’s accuracy was improved by training with a limited number of clinical CTC images. Results: Transfer learning significantly improved the CTC classification accuracy to an average of 99.51%, compared to 96.96% for a model trained solely on pre-trained cell lines (p < 0.05). This approach showed notable efficacy when clinical training images were limited, achieving statistically significant accuracy improvements with as few as 17 clinical CTC images (p < 0.05). Conclusions: Overall, our findings demonstrate that pre-training with cancer cell lines enables rapid and highly accurate automated CTC recognition even with limited clinical data, significantly enhancing clinical applicability and potential utility across diverse cancer diagnostic workflows.
AbstractList Background/Objectives: Circulating tumor cells (CTCs) are important biomarkers for predicting prognosis and evaluating treatment efficacy in cancer. We developed the “CTC-Chip” system based on microfluidics, enabling highly sensitive CTC detection and prognostic assessment in lung cancer and malignant pleural mesothelioma. However, the final identification and enumeration of CTCs require manual intervention, which is time-consuming, prone to human error, and necessitates the involvement of experienced medical professionals. Medical image recognition using machine learning can reduce workload and improve automation. However, CTCs are rare in clinical samples, limiting the training data available to construct a robust CTC image recognition system. In this study, we established a highly accurate artificial intelligence-based CTC recognition system by pre-training convolutional neural networks using images from lung cancer cell lines. Methods: We performed transfer learning of convolutional neural networks. Initially, the models were pre-trained using images obtained from lung cancer cell lines. The model’s accuracy was improved by training with a limited number of clinical CTC images. Results: Transfer learning significantly improved the CTC classification accuracy to an average of 99.51%, compared to 96.96% for a model trained solely on pre-trained cell lines (p < 0.05). This approach showed notable efficacy when clinical training images were limited, achieving statistically significant accuracy improvements with as few as 17 clinical CTC images (p < 0.05). Conclusions: Overall, our findings demonstrate that pre-training with cancer cell lines enables rapid and highly accurate automated CTC recognition even with limited clinical data, significantly enhancing clinical applicability and potential utility across diverse cancer diagnostic workflows.
Circulating tumor cells (CTCs) are rare cancer cells in the blood that can help predict treatment outcomes. However, identifying them manually is slow and needs expertise. In this study, we developed an AI system that accurately detects CTCs using image recognition. To solve the problem of limited clinical images, we first trained the AI system with lung cancer cell line images and then applied transfer learning using a small number of real CTC images. This approach significantly improved accuracy, even with only 17 clinical images. The final model reached 99.5% accuracy. This method reduces the need for large clinical datasets and supports faster, more reliable CTC detection in lung cancer. It may also be applicable to other cancer types and diagnostic workflows. Background/Objectives: Circulating tumor cells (CTCs) are important biomarkers for predicting prognosis and evaluating treatment efficacy in cancer. We developed the “CTC-Chip” system based on microfluidics, enabling highly sensitive CTC detection and prognostic assessment in lung cancer and malignant pleural mesothelioma. However, the final identification and enumeration of CTCs require manual intervention, which is time-consuming, prone to human error, and necessitates the involvement of experienced medical professionals. Medical image recognition using machine learning can reduce workload and improve automation. However, CTCs are rare in clinical samples, limiting the training data available to construct a robust CTC image recognition system. In this study, we established a highly accurate artificial intelligence-based CTC recognition system by pre-training convolutional neural networks using images from lung cancer cell lines. Methods: We performed transfer learning of convolutional neural networks. Initially, the models were pre-trained using images obtained from lung cancer cell lines. The model’s accuracy was improved by training with a limited number of clinical CTC images. Results: Transfer learning significantly improved the CTC classification accuracy to an average of 99.51%, compared to 96.96% for a model trained solely on pre-trained cell lines ( p < 0.05). This approach showed notable efficacy when clinical training images were limited, achieving statistically significant accuracy improvements with as few as 17 clinical CTC images ( p < 0.05). Conclusions: Overall, our findings demonstrate that pre-training with cancer cell lines enables rapid and highly accurate automated CTC recognition even with limited clinical data, significantly enhancing clinical applicability and potential utility across diverse cancer diagnostic workflows.
Circulating tumor cells (CTCs) are rare cancer cells in the blood that can help predict treatment outcomes. However, identifying them manually is slow and needs expertise. In this study, we developed an AI system that accurately detects CTCs using image recognition. To solve the problem of limited clinical images, we first trained the AI system with lung cancer cell line images and then applied transfer learning using a small number of real CTC images. This approach significantly improved accuracy, even with only 17 clinical images. The final model reached 99.5% accuracy. This method reduces the need for large clinical datasets and supports faster, more reliable CTC detection in lung cancer. It may also be applicable to other cancer types and diagnostic workflows.
Circulating tumor cells (CTCs) are important biomarkers for predicting prognosis and evaluating treatment efficacy in cancer. We developed the "CTC-Chip" system based on microfluidics, enabling highly sensitive CTC detection and prognostic assessment in lung cancer and malignant pleural mesothelioma. However, the final identification and enumeration of CTCs require manual intervention, which is time-consuming, prone to human error, and necessitates the involvement of experienced medical professionals. Medical image recognition using machine learning can reduce workload and improve automation. However, CTCs are rare in clinical samples, limiting the training data available to construct a robust CTC image recognition system. In this study, we established a highly accurate artificial intelligence-based CTC recognition system by pre-training convolutional neural networks using images from lung cancer cell lines. We performed transfer learning of convolutional neural networks. Initially, the models were pre-trained using images obtained from lung cancer cell lines. The model's accuracy was improved by training with a limited number of clinical CTC images. Transfer learning significantly improved the CTC classification accuracy to an average of 99.51%, compared to 96.96% for a model trained solely on pre-trained cell lines ( < 0.05). This approach showed notable efficacy when clinical training images were limited, achieving statistically significant accuracy improvements with as few as 17 clinical CTC images ( < 0.05). Overall, our findings demonstrate that pre-training with cancer cell lines enables rapid and highly accurate automated CTC recognition even with limited clinical data, significantly enhancing clinical applicability and potential utility across diverse cancer diagnostic workflows.
Circulating tumor cells (CTCs) are important biomarkers for predicting prognosis and evaluating treatment efficacy in cancer. We developed the "CTC-Chip" system based on microfluidics, enabling highly sensitive CTC detection and prognostic assessment in lung cancer and malignant pleural mesothelioma. However, the final identification and enumeration of CTCs require manual intervention, which is time-consuming, prone to human error, and necessitates the involvement of experienced medical professionals. Medical image recognition using machine learning can reduce workload and improve automation. However, CTCs are rare in clinical samples, limiting the training data available to construct a robust CTC image recognition system. In this study, we established a highly accurate artificial intelligence-based CTC recognition system by pre-training convolutional neural networks using images from lung cancer cell lines.BACKGROUND/OBJECTIVESCirculating tumor cells (CTCs) are important biomarkers for predicting prognosis and evaluating treatment efficacy in cancer. We developed the "CTC-Chip" system based on microfluidics, enabling highly sensitive CTC detection and prognostic assessment in lung cancer and malignant pleural mesothelioma. However, the final identification and enumeration of CTCs require manual intervention, which is time-consuming, prone to human error, and necessitates the involvement of experienced medical professionals. Medical image recognition using machine learning can reduce workload and improve automation. However, CTCs are rare in clinical samples, limiting the training data available to construct a robust CTC image recognition system. In this study, we established a highly accurate artificial intelligence-based CTC recognition system by pre-training convolutional neural networks using images from lung cancer cell lines.We performed transfer learning of convolutional neural networks. Initially, the models were pre-trained using images obtained from lung cancer cell lines. The model's accuracy was improved by training with a limited number of clinical CTC images.METHODSWe performed transfer learning of convolutional neural networks. Initially, the models were pre-trained using images obtained from lung cancer cell lines. The model's accuracy was improved by training with a limited number of clinical CTC images.Transfer learning significantly improved the CTC classification accuracy to an average of 99.51%, compared to 96.96% for a model trained solely on pre-trained cell lines (p < 0.05). This approach showed notable efficacy when clinical training images were limited, achieving statistically significant accuracy improvements with as few as 17 clinical CTC images (p < 0.05).RESULTSTransfer learning significantly improved the CTC classification accuracy to an average of 99.51%, compared to 96.96% for a model trained solely on pre-trained cell lines (p < 0.05). This approach showed notable efficacy when clinical training images were limited, achieving statistically significant accuracy improvements with as few as 17 clinical CTC images (p < 0.05).Overall, our findings demonstrate that pre-training with cancer cell lines enables rapid and highly accurate automated CTC recognition even with limited clinical data, significantly enhancing clinical applicability and potential utility across diverse cancer diagnostic workflows.CONCLUSIONSOverall, our findings demonstrate that pre-training with cancer cell lines enables rapid and highly accurate automated CTC recognition even with limited clinical data, significantly enhancing clinical applicability and potential utility across diverse cancer diagnostic workflows.
Audience Academic
Author Matsumiya, Hiroki
Yoshino, Yuki
Kuwata, Taiji
Nemoto, Yukiko
Kuroda, Koji
Kishi, Yusuke
Kanayama, Masatoshi
Takenaka, Masaru
Yoneda, Kazue
Mori, Masataka
Sasaki, Tohru
Terabayashi, Kenji
Ohnaga, Takashi
Tanaka, Fumihiro
Oyama, Rintaro
Nishizawa, Natsumasa
Honda, Yohei
Chikaishi, Yasuhiro
AuthorAffiliation 1 Second Department of Surgery, School of Medicine, University of Occupational and Environmental Health, Kitakyushu 807-8555, Japan; masataka-m@med.uoeh-u.ac.jp (M.M.); masatoshi-kanayama@med.uoeh-u.ac.jp (M.K.); rintarooyama@med.uoeh-u.ac.jp (R.O.); yukikofukuichi@med.uoeh-u.ac.jp (Y.N.); nmasamed@med.uoeh-u.ac.jp (N.N.); yoheihonda@med.uoeh-u.ac.jp (Y.H.); t-kuwata@med.uoeh-u.ac.jp (T.K.); m-takenaka@med.uoeh-u.ac.jp (M.T.); cywmd0k2@med.uoeh-u.ac.jp (Y.C.); yoneda@med.uoeh-u.ac.jp (K.Y.); kuroda-k@med.uoeh-u.ac.jp (K.K.); ohnaga@pe.ctt.ne.jp (T.O.); ftanaka@med.uoeh-u.ac.jp (F.T.)
2 Department of Mechanical and Intellectual Systems Engineering, Faculty of Engineering, University of Toyama, Toyama 930-8555, Japan; tera@eng.u-toyama.ac.jp (K.T.); yusuke.kishi1@konicaminolta.com (Y.K.); y.yoshino@shimz.co.jp (Y.Y.); tsasaki@eng.u-toyama.ac.jp (T.S.)
AuthorAffiliation_xml – name: 2 Department of Mechanical and Intellectual Systems Engineering, Faculty of Engineering, University of Toyama, Toyama 930-8555, Japan; tera@eng.u-toyama.ac.jp (K.T.); yusuke.kishi1@konicaminolta.com (Y.K.); y.yoshino@shimz.co.jp (Y.Y.); tsasaki@eng.u-toyama.ac.jp (T.S.)
– name: 1 Second Department of Surgery, School of Medicine, University of Occupational and Environmental Health, Kitakyushu 807-8555, Japan; masataka-m@med.uoeh-u.ac.jp (M.M.); masatoshi-kanayama@med.uoeh-u.ac.jp (M.K.); rintarooyama@med.uoeh-u.ac.jp (R.O.); yukikofukuichi@med.uoeh-u.ac.jp (Y.N.); nmasamed@med.uoeh-u.ac.jp (N.N.); yoheihonda@med.uoeh-u.ac.jp (Y.H.); t-kuwata@med.uoeh-u.ac.jp (T.K.); m-takenaka@med.uoeh-u.ac.jp (M.T.); cywmd0k2@med.uoeh-u.ac.jp (Y.C.); yoneda@med.uoeh-u.ac.jp (K.Y.); kuroda-k@med.uoeh-u.ac.jp (K.K.); ohnaga@pe.ctt.ne.jp (T.O.); ftanaka@med.uoeh-u.ac.jp (F.T.)
Author_xml – sequence: 1
  givenname: Hiroki
  surname: Matsumiya
  fullname: Matsumiya, Hiroki
– sequence: 2
  givenname: Kenji
  surname: Terabayashi
  fullname: Terabayashi, Kenji
– sequence: 3
  givenname: Yusuke
  surname: Kishi
  fullname: Kishi, Yusuke
– sequence: 4
  givenname: Yuki
  surname: Yoshino
  fullname: Yoshino, Yuki
– sequence: 5
  givenname: Masataka
  surname: Mori
  fullname: Mori, Masataka
– sequence: 6
  givenname: Masatoshi
  orcidid: 0000-0001-8812-1787
  surname: Kanayama
  fullname: Kanayama, Masatoshi
– sequence: 7
  givenname: Rintaro
  surname: Oyama
  fullname: Oyama, Rintaro
– sequence: 8
  givenname: Yukiko
  surname: Nemoto
  fullname: Nemoto, Yukiko
– sequence: 9
  givenname: Natsumasa
  orcidid: 0000-0002-0749-8871
  surname: Nishizawa
  fullname: Nishizawa, Natsumasa
– sequence: 10
  givenname: Yohei
  surname: Honda
  fullname: Honda, Yohei
– sequence: 11
  givenname: Taiji
  surname: Kuwata
  fullname: Kuwata, Taiji
– sequence: 12
  givenname: Masaru
  orcidid: 0000-0002-4436-2850
  surname: Takenaka
  fullname: Takenaka, Masaru
– sequence: 13
  givenname: Yasuhiro
  surname: Chikaishi
  fullname: Chikaishi, Yasuhiro
– sequence: 14
  givenname: Kazue
  orcidid: 0000-0001-7142-2743
  surname: Yoneda
  fullname: Yoneda, Kazue
– sequence: 15
  givenname: Koji
  surname: Kuroda
  fullname: Kuroda, Koji
– sequence: 16
  givenname: Takashi
  surname: Ohnaga
  fullname: Ohnaga, Takashi
– sequence: 17
  givenname: Tohru
  surname: Sasaki
  fullname: Sasaki, Tohru
– sequence: 18
  givenname: Fumihiro
  surname: Tanaka
  fullname: Tanaka, Fumihiro
BackLink https://www.ncbi.nlm.nih.gov/pubmed/40723173$$D View this record in MEDLINE/PubMed
BookMark eNptkk9r3DAQxU1JadI0596KoJdenOif7dWpLCbtBhZa2u1ZjLVjr4ItpZId2C_Rz1w5SZdsqHTQoPebJz2Yt9mJ8w6z7D2jl0IoemXAGQyRVUxyvlCvsjNOK56XpZInz-rT7CLGW5qWEKwqqzfZqUxaqsVZ9uc6jtD0Nu6s6wiQle12_Z4sjZkCjEhqG8zUwzirm2nwgdTY9-RmgA7JDzS-c3a03pGf-zjiQNpErKYBHFlPqaV--CJp9uR7wHwTwLrZyR_LD5Zr6zC-y1630Ee8eDrPs19frjf1Kl9_-3pTL9e5kbIYc6kMVSk3x6ZBVVXAuGKKQVMq1bYK-QIUlLxd0FY2VBSFKhMISgLdGoMLcZ59fvS9m5oBtwbdGKDXd8EOEPbag9XHirM73fl7zThXQkiaHD49OQT_e8I46sFGk4KAQz9FLbiQgnFZzI99fIHe-im4lG-mBKNCJfZAddCjtq716WEzm-rloqC0olLxRF3-h0p7i4M1aT5am-6PGj48T3qI-G8EEnD1CJjgYwzYHhBG9Txn-sWcib8wn8Wq
Cites_doi 10.1016/j.media.2022.102444
10.1158/1078-0432.CCR-06-1695
10.1007/s12154-013-0094-5
10.1038/s41598-020-69056-1
10.21037/tlcr-22-712
10.1111/cas.15255
10.3389/fbioe.2020.00897
10.1109/ISM.2015.126
10.1038/s42256-020-0153-x
10.3892/ol.2023.13906
10.1007/s10544-013-9775-7
10.1186/s13073-020-00728-3
10.3390/ijms21041475
10.1038/nrc3820
10.1158/1078-0432.CCR-09-1095
10.1016/j.ymeth.2010.01.027
10.1186/s40537-023-00727-2
10.3892/or.2016.5235
10.1038/nature14539
10.1186/s12943-021-01392-w
10.1530/ERC-21-0179
10.3389/fonc.2021.686365
10.1002/cyto.a.22993
10.1158/1078-0432.CCR-04-0378
10.3389/fonc.2021.734959
10.1117/1.JBO.30.S1.S13709
10.3389/fonc.2024.1411731
10.1158/0008-5472.CAN-18-0653
10.1016/j.canlet.2006.12.014
10.1109/TSMC.1979.4310076
10.3389/fcell.2021.666156
10.2147/OTT.S249063
10.7150/thno.5195
ContentType Journal Article
Copyright COPYRIGHT 2025 MDPI AG
2025 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
2025 by the authors. 2025
Copyright_xml – notice: COPYRIGHT 2025 MDPI AG
– notice: 2025 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
– notice: 2025 by the authors. 2025
DBID AAYXX
CITATION
NPM
3V.
7T5
7TO
7XB
8FE
8FH
8FK
8G5
ABUWG
AFKRA
AZQEC
BBNVY
BENPR
BHPHI
CCPQU
DWQXO
GNUQQ
GUQSH
H94
HCIFZ
LK8
M2O
M7P
MBDVC
PHGZM
PHGZT
PIMPY
PKEHL
PQEST
PQGLB
PQQKQ
PQUKI
Q9U
7X8
5PM
DOI 10.3390/cancers17142289
DatabaseName CrossRef
PubMed
ProQuest Central (Corporate)
Immunology Abstracts
Oncogenes and Growth Factors Abstracts
ProQuest Central (purchase pre-March 2016)
ProQuest SciTech Collection
ProQuest Natural Science Journals
ProQuest Central (Alumni) (purchase pre-March 2016)
ProQuest Research Library
ProQuest Central (Alumni)
ProQuest Central UK/Ireland
ProQuest Central Essentials Local Electronic Collection Information
Biological Science Database
ProQuest Central
Natural Science Collection
ProQuest One Community College
ProQuest Central Korea
ProQuest Central Student
ProQuest Research Library
AIDS and Cancer Research Abstracts
ProQuest SciTech Premium Collection
Biological Sciences
ProQuest Research Library
Biological Science Database
Research Library (Corporate)
ProQuest Central Premium
ProQuest One Academic (New)
ProQuest Publicly Available Content Database
ProQuest One Academic Middle East (New)
ProQuest One Academic Eastern Edition (DO NOT USE)
ProQuest One Applied & Life Sciences
ProQuest One Academic
ProQuest One Academic UKI Edition
ProQuest Central Basic
MEDLINE - Academic
PubMed Central (Full Participant titles)
DatabaseTitle CrossRef
PubMed
Publicly Available Content Database
Research Library Prep
ProQuest Central Student
Oncogenes and Growth Factors Abstracts
ProQuest One Academic Middle East (New)
ProQuest Central Essentials
ProQuest Central (Alumni Edition)
SciTech Premium Collection
ProQuest One Community College
Research Library (Alumni Edition)
ProQuest Natural Science Collection
ProQuest Central
ProQuest One Applied & Life Sciences
Natural Science Collection
ProQuest Central Korea
Biological Science Collection
AIDS and Cancer Research Abstracts
ProQuest Research Library
ProQuest Central (New)
ProQuest Biological Science Collection
ProQuest Central Basic
ProQuest One Academic Eastern Edition
Biological Science Database
ProQuest SciTech Collection
ProQuest One Academic UKI Edition
Immunology Abstracts
ProQuest One Academic
ProQuest One Academic (New)
ProQuest Central (Alumni)
MEDLINE - Academic
DatabaseTitleList Publicly Available Content Database


PubMed
MEDLINE - Academic
CrossRef
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: BENPR
  name: ProQuest Central
  url: http://www.proquest.com/pqcentral?accountid=15518
  sourceTypes: Aggregation Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
EISSN 2072-6694
ExternalDocumentID PMC12293340
A850070492
40723173
10_3390_cancers17142289
Genre Journal Article
GeographicLocations Japan
United States--US
GeographicLocations_xml – name: Japan
– name: United States--US
GrantInformation_xml – fundername: Grant-in-Aid for Scientific Research
  grantid: grant number 19K09293
GroupedDBID ---
53G
5VS
8FE
8FH
8G5
AADQD
AAFWJ
AAYXX
ABDBF
ABUWG
ACUHS
ADBBV
AFKRA
AFZYC
ALMA_UNASSIGNED_HOLDINGS
AOIJS
AZQEC
BAWUL
BBNVY
BCNDV
BENPR
BHPHI
BPHCQ
CCPQU
CITATION
DIK
DWQXO
E3Z
EBD
ESX
GNUQQ
GUQSH
GX1
HCIFZ
HYE
IAO
IHR
ITC
KQ8
LK8
M2O
M7P
MODMG
M~E
OK1
P6G
PGMZT
PHGZM
PHGZT
PIMPY
PQGLB
PQQKQ
PROAC
PUEGO
RPM
TUS
NPM
3V.
7T5
7TO
7XB
8FK
H94
M48
MBDVC
PKEHL
PQEST
PQUKI
Q9U
7X8
5PM
ID FETCH-LOGICAL-c445t-49c091712ebbe977a129191ab699ff9e28a9a62f80f4b035596bbea94a0dcce83
IEDL.DBID BENPR
ISSN 2072-6694
IngestDate Thu Aug 21 18:24:32 EDT 2025
Fri Sep 05 15:33:28 EDT 2025
Fri Aug 01 05:20:46 EDT 2025
Wed Aug 13 23:55:47 EDT 2025
Tue Aug 12 03:41:22 EDT 2025
Sat Aug 02 01:41:03 EDT 2025
Wed Sep 10 05:45:04 EDT 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 14
Keywords lung cancer
tumor cell
transfer learning
cell lines
artificial intelligence
Language English
License https://creativecommons.org/licenses/by/4.0
Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c445t-49c091712ebbe977a129191ab699ff9e28a9a62f80f4b035596bbea94a0dcce83
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
ORCID 0000-0002-4436-2850
0000-0002-0749-8871
0000-0001-8812-1787
0000-0001-7142-2743
OpenAccessLink https://www.proquest.com/docview/3233103934?pq-origsite=%requestingapplication%&accountid=15518
PMID 40723173
PQID 3233103934
PQPubID 2032421
ParticipantIDs pubmedcentral_primary_oai_pubmedcentral_nih_gov_12293340
proquest_miscellaneous_3234312458
proquest_journals_3233103934
gale_infotracmisc_A850070492
gale_infotracacademiconefile_A850070492
pubmed_primary_40723173
crossref_primary_10_3390_cancers17142289
PublicationCentury 2000
PublicationDate 2025-07-09
PublicationDateYYYYMMDD 2025-07-09
PublicationDate_xml – month: 07
  year: 2025
  text: 2025-07-09
  day: 09
PublicationDecade 2020
PublicationPlace Switzerland
PublicationPlace_xml – name: Switzerland
– name: Basel
PublicationTitle Cancers
PublicationTitleAlternate Cancers (Basel)
PublicationYear 2025
Publisher MDPI AG
MDPI
Publisher_xml – name: MDPI AG
– name: MDPI
References Toratani (ref_19) 2018; 78
Xu (ref_2) 2021; 20
Otsu (ref_29) 1979; 9
ref_33
Akashi (ref_28) 2023; 26
Aceto (ref_1) 2020; 12
ref_30
Childs (ref_6) 2021; 28
ref_17
Benali (ref_25) 2007; 253
Allard (ref_10) 2004; 10
Lannin (ref_18) 2016; 89
Alzubaidi (ref_32) 2023; 10
Kanayama (ref_15) 2022; 113
Chen (ref_22) 2022; 79
Chen (ref_5) 2020; 13
Sandri (ref_26) 2010; 50
Pantel (ref_27) 2014; 14
Chikaishi (ref_14) 2017; 37
Riethdort (ref_11) 2007; 13
ref_23
ref_21
LeCun (ref_31) 2015; 521
Ohnaga (ref_13) 2013; 15
Toseland (ref_16) 2013; 6
Hamilton (ref_3) 2023; 12
Zeune (ref_20) 2020; 2
Tanaka (ref_12) 2009; 15
Hong (ref_24) 2013; 3
ref_9
ref_8
ref_4
ref_7
References_xml – volume: 79
  start-page: 102444
  year: 2022
  ident: ref_22
  article-title: Recent advances and clinical applications of deep learning in medical image analysis
  publication-title: Med. Image Anal.
  doi: 10.1016/j.media.2022.102444
– volume: 13
  start-page: 920
  year: 2007
  ident: ref_11
  article-title: Detection of circulating tumor cells in peripheral blood of patients with metastatic breast cancer: A validation study of the CellSearch System
  publication-title: Clin. Cancer Res.
  doi: 10.1158/1078-0432.CCR-06-1695
– volume: 6
  start-page: 85
  year: 2013
  ident: ref_16
  article-title: Fluorescent labeling and modification of proteins
  publication-title: J. Chem. Biol.
  doi: 10.1007/s12154-013-0094-5
– ident: ref_21
  doi: 10.1038/s41598-020-69056-1
– volume: 12
  start-page: 877
  year: 2023
  ident: ref_3
  article-title: Significance of circulating tumor cells in lung cancer: A narrative review
  publication-title: Transl. Lung Cancer Res.
  doi: 10.21037/tlcr-22-712
– volume: 113
  start-page: 1028
  year: 2022
  ident: ref_15
  article-title: Prognostic impact of circulating tumor cells detected with the microfluidic “universal CTC-chip” for primary lung cancer
  publication-title: Cancer Sci.
  doi: 10.1111/cas.15255
– ident: ref_23
  doi: 10.3389/fbioe.2020.00897
– ident: ref_30
  doi: 10.1109/ISM.2015.126
– volume: 2
  start-page: 124
  year: 2020
  ident: ref_20
  article-title: Deep learning of circulating tumour cells
  publication-title: Nat. Mach. Intell.
  doi: 10.1038/s42256-020-0153-x
– volume: 26
  start-page: 320
  year: 2023
  ident: ref_28
  article-title: The use of an artificial intelligence algorithm for circulating tumor cell detection in patients with esophageal cancer
  publication-title: Oncol. Lett.
  doi: 10.3892/ol.2023.13906
– volume: 15
  start-page: 611
  year: 2013
  ident: ref_13
  article-title: Polymeric microfluidic devices exhibiting sufficient capture of cancer cell line for isolation of circulating tumor cells
  publication-title: Biomed. Microdevices
  doi: 10.1007/s10544-013-9775-7
– volume: 12
  start-page: 31
  year: 2020
  ident: ref_1
  article-title: Tracking cancer progression: From circulating tumor cells to metastasis
  publication-title: Genome Med.
  doi: 10.1186/s13073-020-00728-3
– ident: ref_9
  doi: 10.3390/ijms21041475
– volume: 14
  start-page: 623
  year: 2014
  ident: ref_27
  article-title: Challenges in circulating tumour cell research
  publication-title: Nat. Rev. Cancer
  doi: 10.1038/nrc3820
– volume: 15
  start-page: 6980
  year: 2009
  ident: ref_12
  article-title: Circulating tumor cell as a diagnostic marker in primary lung cancer
  publication-title: Clin. Cancer Res.
  doi: 10.1158/1078-0432.CCR-09-1095
– volume: 50
  start-page: 289
  year: 2010
  ident: ref_26
  article-title: Circulating tumour cells in clinical practice: Methods of detection and possible characterization
  publication-title: Methods
  doi: 10.1016/j.ymeth.2010.01.027
– volume: 10
  start-page: 46
  year: 2023
  ident: ref_32
  article-title: A survey on deep learning tools dealing with data scarcity: Definitions, challenges, solutions, tips, and applications
  publication-title: J. Big Data.
  doi: 10.1186/s40537-023-00727-2
– volume: 37
  start-page: 77
  year: 2017
  ident: ref_14
  article-title: EpCAM-independent capture of circulating tumor cells with a ‘universal CTC-chip’
  publication-title: Oncol. Rep.
  doi: 10.3892/or.2016.5235
– volume: 521
  start-page: 436
  year: 2015
  ident: ref_31
  article-title: Deep learning
  publication-title: Nature
  doi: 10.1038/nature14539
– volume: 20
  start-page: 104
  year: 2021
  ident: ref_2
  article-title: Using single-cell sequencing technology to detect circulating tumor cells in solid tumors
  publication-title: Mol. Cancer
  doi: 10.1186/s12943-021-01392-w
– volume: 28
  start-page: 631
  year: 2021
  ident: ref_6
  article-title: Whole-genome sequencing of single circulating tumor cells from neuroendocrine neoplasms
  publication-title: Endocr. Relat. Cancer
  doi: 10.1530/ERC-21-0179
– ident: ref_7
  doi: 10.3389/fonc.2021.686365
– volume: 89
  start-page: 922
  year: 2016
  ident: ref_18
  article-title: Comparison and optimization of machine learning methods for automated classification of circulating tumor cells
  publication-title: Cytom. A.
  doi: 10.1002/cyto.a.22993
– volume: 10
  start-page: 6897
  year: 2004
  ident: ref_10
  article-title: Tumor cells circulate in the peripheral blood of all major carcinomas but not in healthy subjects or patients with nonmalignant diseases
  publication-title: Clin. Cancer Res.
  doi: 10.1158/1078-0432.CCR-04-0378
– ident: ref_33
  doi: 10.3389/fonc.2021.734959
– ident: ref_17
  doi: 10.1117/1.JBO.30.S1.S13709
– ident: ref_4
  doi: 10.3389/fonc.2024.1411731
– volume: 78
  start-page: 6703
  year: 2018
  ident: ref_19
  article-title: A convolutional neural network uses microscopic images to differentiate between mouse and human cell lines and their radioresistant clones
  publication-title: Cancer Res.
  doi: 10.1158/0008-5472.CAN-18-0653
– volume: 253
  start-page: 180
  year: 2007
  ident: ref_25
  article-title: Circulating tumor cells (CTC) detection: Clinical impact and future directions
  publication-title: Cancer Lett.
  doi: 10.1016/j.canlet.2006.12.014
– volume: 9
  start-page: 62
  year: 1979
  ident: ref_29
  article-title: A threshold selection method from gray-level histograms
  publication-title: IEEE Trans. Syst. Man Cybern.
  doi: 10.1109/TSMC.1979.4310076
– ident: ref_8
  doi: 10.3389/fcell.2021.666156
– volume: 13
  start-page: 4943
  year: 2020
  ident: ref_5
  article-title: HMGA1 regulates the stem cell-like properties of circulating tumor cells from GIST patients via Wnt/β-catenin pathway
  publication-title: Onco Targets Ther.
  doi: 10.2147/OTT.S249063
– volume: 3
  start-page: 377
  year: 2013
  ident: ref_24
  article-title: Detecting circulating tumor cells: Current challenges and new trends
  publication-title: Theranostics
  doi: 10.7150/thno.5195
SSID ssj0000331767
Score 2.3686128
Snippet Background/Objectives: Circulating tumor cells (CTCs) are important biomarkers for predicting prognosis and evaluating treatment efficacy in cancer. We...
Circulating tumor cells (CTCs) are important biomarkers for predicting prognosis and evaluating treatment efficacy in cancer. We developed the "CTC-Chip"...
Circulating tumor cells (CTCs) are rare cancer cells in the blood that can help predict treatment outcomes. However, identifying them manually is slow and...
SourceID pubmedcentral
proquest
gale
pubmed
crossref
SourceType Open Access Repository
Aggregation Database
Index Database
StartPage 2289
SubjectTerms Accuracy
Algorithms
Antibodies
Artificial intelligence
Automation
Care and treatment
Cells
Classification
Datasets
Deep learning
Development and progression
Diagnosis
Enumeration
Health aspects
Lung cancer
Machine learning
Medical imaging
Medical personnel
Medical research
Mesothelioma
Metastasis
Microfluidics
Mutation
Neural networks
Risk factors
Software
Statistical analysis
Testing
Training
Transfer learning
Tumor cell lines
Tumor cells
Tumors
Viral antibodies
Title Establishing a Highly Accurate Circulating Tumor Cell Image Recognition System for Human Lung Cancer by Pre-Training on Lung Cancer Cell Lines
URI https://www.ncbi.nlm.nih.gov/pubmed/40723173
https://www.proquest.com/docview/3233103934
https://www.proquest.com/docview/3234312458
https://pubmed.ncbi.nlm.nih.gov/PMC12293340
Volume 17
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV1La9wwEB7ygNJL6btO06BCob2IeGXZlg6lbJdN05IsIWxgb0aSZRrY2Kmze8ifyG_ujB_bdQ49j_zSjEbfjEffAHwyqXZhbnMehbnkUrmQqyQVXNpQudRhyBHT4eTzWXJ6JX8t4sUOzPqzMFRW2fvExlHnlaMc-XEkImqJpSP57fYPp65R9He1b6FhutYK-deGYmwX9tElK7T7_e_T2cXlJusS4k3SJG05fiKM948dTW59R33AhaBm71vb02MnvbVLDSsot7akk-fwrMOSbNwq_wXs-PIlPDnv_pa_gocpQr8-y8QMo5qO5T0bO7cmggg2ua5d070LpfP1TVWziV8u2c8b9DHssq8sqkrW0pozxLesSfqzM3QRbNJ8E7P37KL2fN71mmDVUNzc8oyK61_D1cl0PjnlXf8F7qSMV1yiGjGaGwlvrUecaBAbYHhnbKJ1UWgvlNEmEYUKC1QtAhed4ECjpQlz57yK3sBeWZX-HTCnR9YIi2CmENKlkSkQOeVFnMtC2TyJA_jST3t229JsZBiekIayRxoK4DOpJaMFiHPvTHeOAB9EVFbZWMXEYSS1COBwMBIXjhuKe8Vm3cK9y_6ZWQAfN2K6korRSl-tmzEIu4SMVQBvWzvYvDTxzaGJRQGogYVsBhCd91BSXv9uaL1HAqFXJMOD_7_Xe3gqqAcxpZj1Ieyt6rX_gMBoZY86az-C3R-L0V9YQBEN
linkProvider ProQuest
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1Lb9NAEB6VVAIuiDeGAosEgotVZ3f92EOFQkiV0CSqqlTqzazXa1EptUseQvkT_CR-GzN-hLgHbj3vxll7ZuexO_N9AO91qIyXJqkrvFS6MjKeGwUhd2XiRSY0mHL41Jw8mQbDc_ntwr_Ygz9NLwyVVTY2sTTUaWHojPxQcEGUWErIz9c_XWKNotvVhkJD19QK6VEJMVY3dpzYzS9M4ZZHo68o7w-cHw9m_aFbswy4Rkp_5UpcLOYsXW6TxGI0pNEDYhKjk0CpLFOWR1rpgGeRl-ELoHtWAU7USmovNcZGAp97B_Yldbh2YP_LYHp6tj3l8XDRYRBWmEJCKO_QkDAXS-Id55zI5Xfc4U2nsOMV2xWbOy7w-CE8qGNX1quU7RHs2fwx3J3Ut_NP4PcAQ83mVItpRjUk8w3rGbMmQArWv1yYki0MR2frq2LB-nY-Z6MrtGnsrKlkKnJWwagzjKdZecnAxmiSWL98J5Zs2OnCurOa24IV7eHykWMq5n8K57ciiWfQyYvcvgBmVDfRPMHgKePShEJnGKmlmZ_KLErSwHfgU_PZ4-sK1iPGdIgkFN-QkAMfSSwxbXj89kbXfQv4RwSdFfcinzCTpOIOHLRm4kY17eFGsHFtKJbxP7V24N12mH5JxW-5LdblHAzzuPQjB55XerBdNOHboYoJB6KWhmwnEHx4eyS__FHCiHc5hnpCei__v663cG84m4zj8Wh68gruc-I_puNtdQCd1WJtX2NQtkre1JrP4Pttb7a_mDRNVw
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1bb9MwFD4anTTxgrgvMMBIIHiJmjrOxQ8TKl2rlXVVNXXS3oLjOGJSl4y0Feqf4Ifxqzgnl9Lsgbc920nsnONzsY-_D-CDCqR2kjixXScRtgi1Y4d-wG0RO6EONKYcHl1OPp_6p5fi25V3tQd_mrswVFbZ2MTSUCe5pj3yrstdosSSruimdVnE7GT05fanTQxSdNLa0GmommYhOS7hxupLHmdm8wvTueXx-ARl_5Hz0XA-OLVrxgFbC-GtbIEDx_ylx00cG4yMFHpDTGhU7EuZptLwUEnl8zR0UpwMumrpY0clhXISrU3o4nsfwH6AXlJ0YP_rcDq72O74ODiBwA8qfCHXlU5Xk2CLJXGQc05E8zuu8a6D2PGQ7erNHXc4egyP6jiW9SvFewJ7JnsKB-f1Sf0z-D3EsLPZ4WKKUT3JYsP6Wq8JnIINrgtdModh63x9kxdsYBYLNr5B-8YumqqmPGMVpDrD2JqVBw5sguaJDco5sXjDZoWx5zXPBcvbzeUrJ1TY_xwu70USL6CT5Zk5BKZlL1Y8xkAq5UIHrkoxaktSLxFpGCe-Z8Hn5rdHtxXER4SpEUkouiMhCz6RWCJa_PjvtarvMOCHCEYr6oce4ScJyS04avXERavbzY1go9poLKN_Km7B-20zPUmFcJnJ12UfDPm48EILXlZ6sB00Yd2hirkWhC0N2XYgKPF2S3b9o4QU73EM-1zhvPr_uN7BAS66aDKenr2Gh5yokGmnWx5BZ1WszRuMz1bx21rxGXy_77X2F8bgUYM
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Establishing+a+Highly+Accurate+Circulating+Tumor+Cell+Image+Recognition+System+for+Human+Lung+Cancer+by+Pre-Training+on+Lung+Cancer+Cell+Lines&rft.jtitle=Cancers&rft.au=Matsumiya+Hiroki&rft.au=Terabayashi+Kenji&rft.au=Kishi+Yusuke&rft.au=Yoshino+Yuki&rft.date=2025-07-09&rft.pub=MDPI+AG&rft.eissn=2072-6694&rft.volume=17&rft.issue=14&rft.spage=2289&rft_id=info:doi/10.3390%2Fcancers17142289&rft.externalDBID=HAS_PDF_LINK
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=2072-6694&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=2072-6694&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=2072-6694&client=summon