High expression of CDCA7 predicts tumor progression and poor prognosis in human colorectal cancer
Colorectal cancer (CRC) is one of the most fatal types of cancer worldwide. This study aimed to determine the predictive and prognostic values of cell division cycle associated protein 7 (CDCA7) in CRC. Firstly, the relationship between CDCA7 and CRC was assessed through bioinformatics analysis. Sub...
Saved in:
Published in: | Molecular medicine reports Vol. 22; no. 1; pp. 57 - 66 |
---|---|
Main Authors: | , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Greece
Spandidos Publications
01-07-2020
Spandidos Publications UK Ltd D.A. Spandidos |
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Abstract | Colorectal cancer (CRC) is one of the most fatal types of cancer worldwide. This study aimed to determine the predictive and prognostic values of cell division cycle associated protein 7 (CDCA7) in CRC. Firstly, the relationship between CDCA7 and CRC was assessed through bioinformatics analysis. Subsequently, CDCA7 expression levels were detected in various CRC cell lines, as well as 15 fresh human CRC tissues and their paired adjacent normal colorectal tissues using reverse transcription‑quantitative PCR and western blotting. Additionally, immunohistochemical staining was used to determine the levels of CDCA7 in 104 CRC tissues and their paired adjacent normal colorectal tissues. The present study revealed that CDCA7 expression was upregulated in CRC tissues and cell lines. The positive expression rates of CDCA7 in normal and CRC tissues were 26.92 and 75.96%, respectively. The intensities of CDCA7 immunostaining were significantly associated with CRC invasion depth, lymph node metastasis, tumor‑node‑metastasis stage and distant metastasis. However, no significant differences in sex, age, tumor size and CRC differentiation were found between high and low CDCA7 expression groups. Furthermore, patients with low CDCA7 expression exhibited a greater overall survival rate of CRC compared to those with high CDCA7 expression. The findings of this study indicated that CDCA7 may serve a significant role in CRC prognosis and progression, and may be considered a novel biomarker for the prediction of patient survival after colectomy. |
---|---|
AbstractList | Colorectal cancer (CRC) is one of the most fatal types of cancer worldwide. This study aimed to determine the predictive and prognostic values of cell division cycle associated protein 7 (CDCA7) in CRC. Firstly, the relationship between CDCA7 and CRC was assessed through bioinformatics analysis. Subsequently, CDCA7 expression levels were detected in various CRC cell lines, as well as 15 fresh human CRC tissues and their paired adjacent normal colorectal tissues using reverse transcription-quantitative PCR and western blotting. Additionally, immunohistochemical staining was used to determine the levels of CDCA7 in 104 CRC tissues and their paired adjacent normal colorectal tissues. The present study revealed that CDCA7 expression was upregulated in CRC tissues and cell lines. The positive expression rates of CDCA7 in normal and CRC tissues were 26.92 and 75.96%, respectively. The intensities of CDCA7 immunostaining were significantly associated with CRC invasion depth, lymph node metastasis, tumor-node-metastasis stage and distant metastasis. However, no significant differences in sex, age, tumor size and CRC differentiation were found between high and low CDCA7 expression groups. Furthermore, patients with low CDCA7 expression exhibited a greater overall survival rate of CRC compared to those with high CDCA7 expression. The findings of this study indicated that CDCA7 may serve a significant role in CRC prognosis and progression, and may be considered a novel biomarker for the prediction of patient survival after colectomy. Colorectal cancer (CRC) is one of the most fatal types of cancer worldwide. This study aimed to determine the predictive and prognostic values of cell division cycle associated protein 7 (CDCA7) in CRC. Firstly, the relationship between CDCA7 and CRC was assessed through bioinformatics analysis. Subsequently, CDCA7 expression levels were detected in various CRC cell lines, as well as 15 fresh human CRC tissues and their paired adjacent normal colorectal tissues using reverse transcription-quantitative PCR and western blotting. Additionally, immunohistochemical staining was used to determine the levels of CDCA7 in 104 CRC tissues and their paired adjacent normal colorectal tissues. The present study revealed that CDCA7 expression was upregulated in CRC tissues and cell lines. The positive expression rates of CDCA7 in normal and CRC tissues were 26.92 and 75.96%, respectively. The intensities of CDCA7 immunostaining were significantly associated with CRC invasion depth, lymph node metastasis, tumor-node-metastasis stage and distant metastasis. However, no significant differences in sex, age, tumor size and CRC differentiation were found between high and low CDCA7 expression groups. Furthermore, patients with low CDCA7 expression exhibited a greater overall survival rate of CRC compared to those with high CDCA7 expression. The findings of this study indicated that CDCA7 may serve a significant role in CRC prognosis and progression, and may be considered a novel biomarker for the prediction of patient survival after colectomy. Key words: cell division cycle associated protein 7, colorectal cancer, progression, prognosis, bioinformatics analysis Colorectal cancer (CRC) is one of the most fatal types of cancer worldwide. This study aimed to determine the predictive and prognostic values of cell division cycle associated protein 7 (CDCA7) in CRC. Firstly, the relationship between CDCA7 and CRC was assessed through bioinformatics analysis. Subsequently, CDCA7 expression levels were detected in various CRC cell lines, as well as 15 fresh human CRC tissues and their paired adjacent normal colorectal tissues using reverse transcription‑quantitative PCR and western blotting. Additionally, immunohistochemical staining was used to determine the levels of CDCA7 in 104 CRC tissues and their paired adjacent normal colorectal tissues. The present study revealed that CDCA7 expression was upregulated in CRC tissues and cell lines. The positive expression rates of CDCA7 in normal and CRC tissues were 26.92 and 75.96%, respectively. The intensities of CDCA7 immunostaining were significantly associated with CRC invasion depth, lymph node metastasis, tumor‑node‑metastasis stage and distant metastasis. However, no significant differences in sex, age, tumor size and CRC differentiation were found between high and low CDCA7 expression groups. Furthermore, patients with low CDCA7 expression exhibited a greater overall survival rate of CRC compared to those with high CDCA7 expression. The findings of this study indicated that CDCA7 may serve a significant role in CRC prognosis and progression, and may be considered a novel biomarker for the prediction of patient survival after colectomy. Colorectal cancer (CRC) is one of the most fatal types of cancer worldwide. This study aimed to determine the predictive and prognostic values of cell division cycle associated protein 7 (CDCA7) in CRC. Firstly, the relationship between CDCA7 and CRC was assessed through bioinformatics analysis. Subsequently, CDCA7 expression levels were detected in various CRC cell lines, as well as 15 fresh human CRC tissues and their paired adjacent normal colorectal tissues using reverse transcription‑quantitative PCR and western blotting. Additionally, immunohistochemical staining was used to determine the levels of CDCA7 in 104 CRC tissues and their paired adjacent normal colorectal tissues. The present study revealed that CDCA7 expression was upregulated in CRC tissues and cell lines. The positive expression rates of CDCA7 in normal and CRC tissues were 26.92 and 75.96%, respectively. The intensities of CDCA7 immunostaining were significantly associated with CRC invasion depth, lymph node metastasis, tumor‑node‑metastasis stage and distant metastasis. However, no significant differences in sex, age, tumor size and CRC differentiation were found between high and low CDCA7 expression groups. Furthermore, patients with low CDCA7 expression exhibited a greater overall survival rate of CRC compared to those with high CDCA7 expression. The findings of this study indicated that CDCA7 may serve a significant role in CRC prognosis and progression, and may be considered a novel biomarker for the prediction of patient survival after colectomy.Colorectal cancer (CRC) is one of the most fatal types of cancer worldwide. This study aimed to determine the predictive and prognostic values of cell division cycle associated protein 7 (CDCA7) in CRC. Firstly, the relationship between CDCA7 and CRC was assessed through bioinformatics analysis. Subsequently, CDCA7 expression levels were detected in various CRC cell lines, as well as 15 fresh human CRC tissues and their paired adjacent normal colorectal tissues using reverse transcription‑quantitative PCR and western blotting. Additionally, immunohistochemical staining was used to determine the levels of CDCA7 in 104 CRC tissues and their paired adjacent normal colorectal tissues. The present study revealed that CDCA7 expression was upregulated in CRC tissues and cell lines. The positive expression rates of CDCA7 in normal and CRC tissues were 26.92 and 75.96%, respectively. The intensities of CDCA7 immunostaining were significantly associated with CRC invasion depth, lymph node metastasis, tumor‑node‑metastasis stage and distant metastasis. However, no significant differences in sex, age, tumor size and CRC differentiation were found between high and low CDCA7 expression groups. Furthermore, patients with low CDCA7 expression exhibited a greater overall survival rate of CRC compared to those with high CDCA7 expression. The findings of this study indicated that CDCA7 may serve a significant role in CRC prognosis and progression, and may be considered a novel biomarker for the prediction of patient survival after colectomy. |
Audience | Academic |
Author | Huang, Jiean Zhang, Jinxiu Liao, Cun Qin, Mengbin Li, Siman |
AuthorAffiliation | 1 Department of Gastroenterology, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi 530021, P.R. China 2 Department of Gastroenterology, The Second Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi 530007, P.R. China 3 Department of Colorectal-Anal Surgery, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi 530021, P.R. China |
AuthorAffiliation_xml | – name: 2 Department of Gastroenterology, The Second Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi 530007, P.R. China – name: 3 Department of Colorectal-Anal Surgery, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi 530021, P.R. China – name: 1 Department of Gastroenterology, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi 530021, P.R. China |
Author_xml | – sequence: 1 givenname: Siman surname: Li fullname: Li, Siman organization: Department of Gastroenterology, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi 530021, P.R. China – sequence: 2 givenname: Jiean surname: Huang fullname: Huang, Jiean organization: Department of Gastroenterology, The Second Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi 530007, P.R. China – sequence: 3 givenname: Mengbin surname: Qin fullname: Qin, Mengbin organization: Department of Gastroenterology, The Second Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi 530007, P.R. China – sequence: 4 givenname: Jinxiu surname: Zhang fullname: Zhang, Jinxiu organization: Department of Gastroenterology, The Second Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi 530007, P.R. China – sequence: 5 givenname: Cun surname: Liao fullname: Liao, Cun organization: Department of Colorectal‑Anal Surgery, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi 530021, P.R. China |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/32319649$$D View this record in MEDLINE/PubMed |
BookMark | eNptUkuPFCEYJGaN-9CrR0PixcuM8EHTzcVkMj7WZBMveiY0_THDphtG6Db672V0dn1kAwlQVBV8UJfkLKaIhDznbC06Da-nKa-BAVtzzjr9iFzwVvOVYEyeneagdXtOLku5ZUw10Ogn5FyA4FpJfUHsddjtKX4_ZCwlpEiTp9u3201LKzIENxc6L1PKdZl2dxwbB3pIJzCmEgoNke6XyUbq0pgyutmO1NnoMD8lj70dCz47jVfky_t3n7fXq5tPHz5uNzcrJ7tmXmml-kFooWztCAOoFj1vvLfQDU5ygc6DdE4K2wlo-0GhFD0OzoGuul5ckTe_fQ9LP1Uc45ztaA45TDb_MMkG8-9ODHuzS99MC7KTLa8Gr04GOX1dsMxmCsXhONqIaSkG6u2athH6SH35H_U2LTnW8gxIpptO6gb-sHZ2RBOiT_VcdzQ1GwVaMdkBq6z1A6zaBpyCq7_tQ8UfEricSsno72vkzBxDYWoozDEU5lcoquDF3y9zT79LgfgJ9kq1Hg |
CitedBy_id | crossref_primary_10_1155_2022_2184867 crossref_primary_10_3390_cancers14092084 crossref_primary_10_3389_fgene_2022_900111 crossref_primary_10_3389_fonc_2020_607622 crossref_primary_10_3389_fonc_2021_734655 |
Cites_doi | 10.4238/2015.December.8.4 10.1007/s11626-019-00376-x 10.1016/j.humpath.2018.03.030 10.1074/jbc.M107357200 10.1158/0008-5472.CAN-05-0536 10.1620/tjem.218.129 10.3322/caac.21254 10.1093/nar/gky1015 10.1016/j.bbaexp.2006.02.004 10.1128/MCB.00276-12 10.3322/caac.21262 10.3324/haematol.2018.188961 10.3322/caac.21492 10.3892/ol.2017.5751 10.3892/ol.2017.5820 10.1002/ijc.29210 10.1038/s12276-018-0101-6 10.1074/jbc.275.14.10477 10.1016/j.ccr.2012.08.013 10.1128/MCB.17.9.4967 10.3892/ol.2017.5868 10.1039/C7DT04037G 10.1006/meth.2001.1262 10.1016/j.ajhg.2015.12.013 10.1006/excr.1997.3815 10.1007/s11894-017-0587-4 10.1093/nar/27.1.29 |
ContentType | Journal Article |
Copyright | COPYRIGHT 2020 Spandidos Publications Copyright Spandidos Publications UK Ltd. 2020 Copyright: © Li et al. 2020 |
Copyright_xml | – notice: COPYRIGHT 2020 Spandidos Publications – notice: Copyright Spandidos Publications UK Ltd. 2020 – notice: Copyright: © Li et al. 2020 |
DBID | CGR CUY CVF ECM EIF NPM AAYXX CITATION 3V. 7X7 7XB 88E 8AO 8FE 8FH 8FI 8FJ 8FK ABUWG AFKRA AN0 AZQEC BBNVY BENPR BHPHI CCPQU DWQXO FYUFA GHDGH GNUQQ HCIFZ K9. LK8 M0S M1P M7P PQEST PQQKQ PQUKI PRINS 7X8 5PM |
DOI | 10.3892/mmr.2020.11089 |
DatabaseName | Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed CrossRef ProQuest Central (Corporate) Health & Medical Collection ProQuest Central (purchase pre-March 2016) Medical Database (Alumni Edition) ProQuest Pharma Collection ProQuest SciTech Collection ProQuest Natural Science Collection Hospital Premium Collection Hospital Premium Collection (Alumni Edition) ProQuest Central (Alumni) (purchase pre-March 2016) ProQuest Central (Alumni) ProQuest Central British Nursing Database ProQuest Central Essentials Biological Science Collection ProQuest Databases ProQuest Natural Science Collection ProQuest One Community College ProQuest Central Health Research Premium Collection Health Research Premium Collection (Alumni) ProQuest Central Student SciTech Premium Collection ProQuest Health & Medical Complete (Alumni) Biological Sciences Health & Medical Collection (Alumni Edition) PML(ProQuest Medical Library) Biological Science Database ProQuest One Academic Eastern Edition (DO NOT USE) ProQuest One Academic ProQuest One Academic UKI Edition ProQuest Central China MEDLINE - Academic PubMed Central (Full Participant titles) |
DatabaseTitle | MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) CrossRef ProQuest Central Student ProQuest Central Essentials ProQuest Health & Medical Complete (Alumni) ProQuest Central (Alumni Edition) SciTech Premium Collection ProQuest One Community College ProQuest Natural Science Collection ProQuest Pharma Collection ProQuest Central China ProQuest Central Health Research Premium Collection Health and Medicine Complete (Alumni Edition) Natural Science Collection ProQuest Central Korea Biological Science Collection ProQuest Medical Library (Alumni) ProQuest Biological Science Collection ProQuest One Academic Eastern Edition British Nursing Index with Full Text ProQuest Hospital Collection Health Research Premium Collection (Alumni) Biological Science Database ProQuest SciTech Collection ProQuest Hospital Collection (Alumni) ProQuest Health & Medical Complete ProQuest Medical Library ProQuest One Academic UKI Edition ProQuest One Academic ProQuest Central (Alumni) MEDLINE - Academic |
DatabaseTitleList | ProQuest Central Student MEDLINE MEDLINE - Academic |
Database_xml | – sequence: 1 dbid: ECM name: MEDLINE url: https://search.ebscohost.com/login.aspx?direct=true&db=cmedm&site=ehost-live sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Biology |
EISSN | 1791-3004 |
EndPage | 66 |
ExternalDocumentID | A629604820 10_3892_mmr_2020_11089 32319649 |
Genre | Journal Article |
GeographicLocations | United States |
GeographicLocations_xml | – name: United States |
GroupedDBID | --- 0R~ 123 3V. 53G 7X7 88E 8AO 8FE 8FH 8FI 8FJ ABDBF ABJNI ABUWG ACGFS ACPRK ADBBV AEGXH AENEX AFKRA AHMBA ALIPV ALMA_UNASSIGNED_HOLDINGS AN0 BAWUL BBNVY BENPR BHPHI BNQBC BPHCQ BVXVI C45 CCPQU CGR CS3 CUY CVF DIK DU5 EBS ECM EIF EJD F5P FRP FYUFA H13 HCIFZ HMCUK HUR HZ~ IAO IHR INH INR IPNFZ ITC LK8 M1P M7P NPM O9- OK1 OVD PQQKQ PROAC PSQYO RIG TEORI TR2 UKHRP W2D AAYXX CITATION 7XB 8FK AZQEC DWQXO GNUQQ K9. PQEST PQUKI PRINS 7X8 5PM |
ID | FETCH-LOGICAL-c485t-966bd3936a36ae2d267ef15ffa28dc413ecf24cc43a8327bd6e43bedcc29d39b3 |
ISSN | 1791-2997 1791-3004 |
IngestDate | Tue Sep 17 21:25:21 EDT 2024 Sat Oct 26 04:32:56 EDT 2024 Thu Oct 10 17:00:57 EDT 2024 Tue Nov 19 20:42:19 EST 2024 Tue Nov 12 23:01:37 EST 2024 Fri Aug 23 01:33:03 EDT 2024 Sat Nov 02 12:26:40 EDT 2024 |
IsDoiOpenAccess | true |
IsOpenAccess | true |
IsPeerReviewed | false |
IsScholarly | true |
Issue | 1 |
Keywords | cell division cycle associated protein 7 progression colorectal cancer prognosis bioinformatics analysis |
Language | English |
License | This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
LinkModel | OpenURL |
MergedId | FETCHMERGED-LOGICAL-c485t-966bd3936a36ae2d267ef15ffa28dc413ecf24cc43a8327bd6e43bedcc29d39b3 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Contributed equally |
OpenAccessLink | https://pubmed.ncbi.nlm.nih.gov/PMC7248471 |
PMID | 32319649 |
PQID | 2409584952 |
PQPubID | 2044955 |
PageCount | 10 |
ParticipantIDs | pubmedcentral_primary_oai_pubmedcentral_nih_gov_7248471 proquest_miscellaneous_2393575391 proquest_journals_2409584952 gale_infotracmisc_A629604820 gale_infotracacademiconefile_A629604820 crossref_primary_10_3892_mmr_2020_11089 pubmed_primary_32319649 |
PublicationCentury | 2000 |
PublicationDate | 2020-07-01 |
PublicationDateYYYYMMDD | 2020-07-01 |
PublicationDate_xml | – month: 07 year: 2020 text: 2020-07-01 day: 01 |
PublicationDecade | 2020 |
PublicationPlace | Greece |
PublicationPlace_xml | – name: Greece – name: Athens |
PublicationTitle | Molecular medicine reports |
PublicationTitleAlternate | Mol Med Rep |
PublicationYear | 2020 |
Publisher | Spandidos Publications Spandidos Publications UK Ltd D.A. Spandidos |
Publisher_xml | – name: Spandidos Publications – name: Spandidos Publications UK Ltd – name: D.A. Spandidos |
References | Bray (key20200713235030_b21-mmr-22-01-0057) 2018; 68 Albulescu (key20200713235030_b16-mmr-22-01-0057) 2013; 3 Chiu (key20200713235030_b4-mmr-22-01-0057) 2017; 19 Lu (key20200713235030_b28-mmr-22-01-0057) 2017; 13 Gill (key20200713235030_b29-mmr-22-01-0057) 2013; 33 Cho (key20200713235030_b10-mmr-22-01-0057) 2009; 218 Wang (key20200713235030_b15-mmr-22-01-0057) 2015; 14 Goto (key20200713235030_b25-mmr-22-01-0057) 2006; 1759 Lewis (key20200713235030_b11-mmr-22-01-0057) 1997; 17 GBD 2015 Mortality and Causes of Death Collaborators (key20200713235030_b22-mmr-22-01-0057) 2016; 388 Torre (key20200713235030_b1-mmr-22-01-0057) 2015; 65 Cui (key20200713235030_b6-mmr-22-01-0057) 2019; 83 Tate (key20200713235030_b19-mmr-22-01-0057) 2019; 47 Kitaura (key20200713235030_b24-mmr-22-01-0057) 2000; 275 Wang (key20200713235030_b13-mmr-22-01-0057) 2018; 50 Li (key20200713235030_b30-mmr-22-01-0057) 2019; 55 Prescott (key20200713235030_b9-mmr-22-01-0057) 2001; 276 Osthus (key20200713235030_b17-mmr-22-01-0057) 2005; 65 Cheng (key20200713235030_b18-mmr-22-01-0057) 2016; 98 Conover (key20200713235030_b23-mmr-22-01-0057) 1998; 238 Ferlay (key20200713235030_b3-mmr-22-01-0057) 2015; 136 Calon (key20200713235030_b5-mmr-22-01-0057) 2012; 22 Siegel (key20200713235030_b2-mmr-22-01-0057) 2015; 65 Jiménez-P (key20200713235030_b14-mmr-22-01-0057) 2018; 103 Livak (key20200713235030_b20-mmr-22-01-0057) 2001; 25 Lee (key20200713235030_b27-mmr-22-01-0057) 2017; 13 Ogata (key20200713235030_b7-mmr-22-01-0057) 1999; 27 Basu Baul (key20200713235030_b12-mmr-22-01-0057) 2018; 47 Zhang (key20200713235030_b26-mmr-22-01-0057) 2017; 13 Harris (key20200713235030_b8-mmr-22-01-0057) 2004; 32 |
References_xml | – volume: 14 start-page: 16151 year: 2015 ident: key20200713235030_b15-mmr-22-01-0057 article-title: Identification of hub genes and pathways associated with retinoblastoma based on co-expression network analysis publication-title: Genet Mol Res doi: 10.4238/2015.December.8.4 contributor: fullname: Wang – volume: 55 start-page: 577 year: 2019 ident: key20200713235030_b30-mmr-22-01-0057 article-title: Long noncoding RNA FGD5-AS1 promotes colorectal cancer cell proliferation, migration, and invasion through upregulating CDCA7 via sponging miR-302e publication-title: In Vitro Cell Dev Biol Anim doi: 10.1007/s11626-019-00376-x contributor: fullname: Li – volume: 388 start-page: 1459 issue: (10053) year: 2016 ident: key20200713235030_b22-mmr-22-01-0057 article-title: Global, regional, and national life expectancy, all-cause mortality, and cause-specific mortality for 249 causes of death, 1980–2015: a systematic analysis for the Global Burden of Disease Study 2015 publication-title: Lancet contributor: fullname: GBD 2015 Mortality and Causes of Death Collaborators – volume: 83 start-page: 36 year: 2019 ident: key20200713235030_b6-mmr-22-01-0057 article-title: MMP14 predicts a poor prognosis in patients with colorectal cancer publication-title: Hum Pathol doi: 10.1016/j.humpath.2018.03.030 contributor: fullname: Cui – volume: 276 start-page: 48276 year: 2001 ident: key20200713235030_b9-mmr-22-01-0057 article-title: A novel c-Myc-responsive gene, JPO1, participates in neoplastic transformation publication-title: J Biol Chem doi: 10.1074/jbc.M107357200 contributor: fullname: Prescott – volume: 65 start-page: 5620 year: 2005 ident: key20200713235030_b17-mmr-22-01-0057 article-title: The Myc target gene JPO1/CDCA7 is frequently overexpressed in human tumors and has limited transforming activity in vivo publication-title: Cancer Res doi: 10.1158/0008-5472.CAN-05-0536 contributor: fullname: Osthus – volume: 218 start-page: 129 year: 2009 ident: key20200713235030_b10-mmr-22-01-0057 article-title: Molecular characterization of a new ovarian cancer cell line, YDOV-151, established from mucinous cystadenocarcinoma publication-title: Tohoku J Exp Med doi: 10.1620/tjem.218.129 contributor: fullname: Cho – volume: 65 start-page: 5 year: 2015 ident: key20200713235030_b2-mmr-22-01-0057 article-title: Cancer statistics, 2015 publication-title: CA Cancer J Clin doi: 10.3322/caac.21254 contributor: fullname: Siegel – volume: 47 start-page: D941 year: 2019 ident: key20200713235030_b19-mmr-22-01-0057 article-title: COSMIC: The catalogue of somatic mutations in cancer publication-title: Nucleic Acids Res doi: 10.1093/nar/gky1015 contributor: fullname: Tate – volume: 1759 start-page: 60 year: 2006 ident: key20200713235030_b25-mmr-22-01-0057 article-title: JPO1/CDCA7, a novel transcription factor E2F1-induced protein, possesses intrinsic transcriptional regulator activity publication-title: Biochim Biophys Acta doi: 10.1016/j.bbaexp.2006.02.004 contributor: fullname: Goto – volume: 33 start-page: 498 year: 2013 ident: key20200713235030_b29-mmr-22-01-0057 article-title: The MYC-associated protein CDCA7 is phosphorylated by AKT to regulate MYC-dependent apoptosis and transformation publication-title: Mol Cell Biol doi: 10.1128/MCB.00276-12 contributor: fullname: Gill – volume: 65 start-page: 87 year: 2015 ident: key20200713235030_b1-mmr-22-01-0057 article-title: Global cancer statistics, 2012 publication-title: CA Cancer J Clin doi: 10.3322/caac.21262 contributor: fullname: Torre – volume: 103 start-page: 1669 year: 2018 ident: key20200713235030_b14-mmr-22-01-0057 article-title: CDCA7 is a critical mediator of lymphomagenesis that selectively regulates anchorage-independent growth publication-title: Haematologica doi: 10.3324/haematol.2018.188961 contributor: fullname: Jiménez-P – volume: 68 start-page: 394 issue: (6) year: 2018 ident: key20200713235030_b21-mmr-22-01-0057 article-title: Global Cancer Statistics 2018: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries publication-title: CA Cancer J Clin doi: 10.3322/caac.21492 contributor: fullname: Bray – volume: 13 start-page: 2838 year: 2017 ident: key20200713235030_b28-mmr-22-01-0057 article-title: Oridonin induces G2/M cell cycle arrest and apoptosis via the PI3K/Akt signaling pathway in hormone-independent prostate cancer cells publication-title: Oncol Lett doi: 10.3892/ol.2017.5751 contributor: fullname: Lu – volume: 13 start-page: 2921 year: 2017 ident: key20200713235030_b27-mmr-22-01-0057 article-title: Acetonitrile extract of Salvia miltiorrhizaRadix exhibits growth-inhibitory effects on prostate cancer cells through the induction of cell cycle arrest and apoptosis publication-title: Oncol Lett doi: 10.3892/ol.2017.5820 contributor: fullname: Lee – volume: 32 start-page: D258 issue: (Database Issue) year: 2004 ident: key20200713235030_b8-mmr-22-01-0057 article-title: The Gene Ontology (GO) database and informatics resource publication-title: Nucleic Acids Res contributor: fullname: Harris – volume: 136 start-page: E359 year: 2015 ident: key20200713235030_b3-mmr-22-01-0057 article-title: Cancer incidence and mortality worldwide: Sources, methods and major patterns in GLOBOCAN 2012 publication-title: Int J Cancer doi: 10.1002/ijc.29210 contributor: fullname: Ferlay – volume: 50 start-page: 1 year: 2018 ident: key20200713235030_b13-mmr-22-01-0057 article-title: The EGF/hnRNP Q1 axis is involved in tumorigenesis via the regulation of cell cycle-related genes publication-title: Exp Mol Med doi: 10.1038/s12276-018-0101-6 contributor: fullname: Wang – volume: 3 start-page: 1 year: 2013 ident: key20200713235030_b16-mmr-22-01-0057 article-title: Elevated cyclin B2 expression in invasive breast carcinoma is associated with unfavorable clinical outcome publication-title: BMC Cancer contributor: fullname: Albulescu – volume: 275 start-page: 10477 year: 2000 ident: key20200713235030_b24-mmr-22-01-0057 article-title: Reciprocal regulation via protein-protein interaction between c-Myc and p21(cip1/waf1/sdi1) in DNA replication and transcription publication-title: J Biol Chem doi: 10.1074/jbc.275.14.10477 contributor: fullname: Kitaura – volume: 22 start-page: 571 year: 2012 ident: key20200713235030_b5-mmr-22-01-0057 article-title: Dependency of colorectal cancer on a TGF-β-driven program in stromal cells for metastasis initiation publication-title: Cancer Cell doi: 10.1016/j.ccr.2012.08.013 contributor: fullname: Calon – volume: 17 start-page: 4967 year: 1997 ident: key20200713235030_b11-mmr-22-01-0057 article-title: Identification of putative c-Myc-responsive genes: Characterization of rcl, a novel growth-related gene publication-title: Mol Cell Biol doi: 10.1128/MCB.17.9.4967 contributor: fullname: Lewis – volume: 13 start-page: 3817 year: 2017 ident: key20200713235030_b26-mmr-22-01-0057 article-title: Rnf2 knockdown reduces cell viability and promotes cell cycle arrest in gastric cancer cells publication-title: Oncol Lett doi: 10.3892/ol.2017.5868 contributor: fullname: Zhang – volume: 47 start-page: 1993 year: 2018 ident: key20200713235030_b12-mmr-22-01-0057 article-title: Triphenylstannyl ((arylimino)methyl) benzoates with selective potency that induce G1 and G2/M cell cycle arrest and trigger apoptosis via ROS in human cervical cancer cells publication-title: Dalton Trans doi: 10.1039/C7DT04037G contributor: fullname: Basu Baul – volume: 25 start-page: 402 year: 2001 ident: key20200713235030_b20-mmr-22-01-0057 article-title: Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) method publication-title: Methods doi: 10.1006/meth.2001.1262 contributor: fullname: Livak – volume: 98 start-page: 256 year: 2016 ident: key20200713235030_b18-mmr-22-01-0057 article-title: Whole-genome sequencing reveals diverse models of structural variations in esophageal squamous cell carcinoma publication-title: Am J Hum Genet doi: 10.1016/j.ajhg.2015.12.013 contributor: fullname: Cheng – volume: 238 start-page: 122 year: 1998 ident: key20200713235030_b23-mmr-22-01-0057 article-title: Insulin-like growth factor I induction of c-myc expression in bovine fibroblasts can be blocked by antecedent insulin receptor activation publication-title: Exp Cell Res doi: 10.1006/excr.1997.3815 contributor: fullname: Conover – volume: 19 start-page: 47 year: 2017 ident: key20200713235030_b4-mmr-22-01-0057 article-title: Colorectal cancer screening in Asia publication-title: Curr Gastroenterol Rep doi: 10.1007/s11894-017-0587-4 contributor: fullname: Chiu – volume: 27 start-page: 29 year: 1999 ident: key20200713235030_b7-mmr-22-01-0057 article-title: KEGG: Kyoto Encyclopedia of Genes and Genomes publication-title: Nucleic Acids Res doi: 10.1093/nar/27.1.29 contributor: fullname: Ogata |
SSID | ssj0065259 |
Score | 2.3272495 |
Snippet | Colorectal cancer (CRC) is one of the most fatal types of cancer worldwide. This study aimed to determine the predictive and prognostic values of cell division... |
SourceID | pubmedcentral proquest gale crossref pubmed |
SourceType | Open Access Repository Aggregation Database Index Database |
StartPage | 57 |
SubjectTerms | Adult Age Aged Analysis Antibodies Bioinformatics Cancer Cancer metastasis Cancer research Cell cycle Cell division Colorectal cancer Colorectal carcinoma Colorectal Neoplasms - diagnosis Colorectal Neoplasms - genetics Colorectal Neoplasms - pathology Development and progression Disease Disease Progression DNA methylation Female Gene expression Gene Expression Regulation, Neoplastic Genomes Humans Immunohistochemistry Lymph nodes Lymphatic Metastasis - diagnosis Lymphatic Metastasis - genetics Lymphatic Metastasis - pathology Male Medical prognosis Metastases Metastasis MicroRNAs Middle Aged Neoplasm Invasiveness - diagnosis Neoplasm Invasiveness - genetics Neoplasm Invasiveness - pathology Nuclear Proteins - analysis Nuclear Proteins - genetics Prognosis Proteins Researchers Reverse transcription Scientific equipment industry Transcription factors Tumors Up-Regulation Western blotting |
Title | High expression of CDCA7 predicts tumor progression and poor prognosis in human colorectal cancer |
URI | https://www.ncbi.nlm.nih.gov/pubmed/32319649 https://www.proquest.com/docview/2409584952 https://www.proquest.com/docview/2393575391 https://pubmed.ncbi.nlm.nih.gov/PMC7248471 |
Volume | 22 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV3di9NAEF96J4Iv4rfVU1YQfJBgutl87GNpe_Sueii9A9-W7GaDeWgibQP63zuzm88TRB-EEspkk25nftmZ3cz-hpC3Is4591XqKZb7Hk_90EsEB4PkYH4lfOMzW8R2G199TZYrvppM2voJvey_WhpkYGvcOfsP1u5uCgL4DjaHI1gdjn9ld0zcQN5-l99qg8HFcjGPkQ0gKzB141jvqr1LzGraWLKAqhGWFXKUFGVTvg9ZrXFURB4RRMh-GM5-aovrdu_o25cQXaKPzRbYFrseheu6WaO-LEwv_eLIDDDLVhWdtFvPvizKH0U9XKOACWmbz9quUeIWnaw6jNYi399sBqlLOPjGYuaBe3QO2PQyZAUbjtiM_YZMN_yG8cCRu2out10EBGhIObvbIRksc9sgRO8M2wSA9XwrPy_P5ceLq80JucNgGLMT9otN6-ejkNlSfF2vHSUo3v_D-O6jkOe24x9EPuOs3EGYc_2A3G_mJ3TugPWQTEz5iNx1FUt_PiYpwov28KJVTi28aAsvauFFB_CiYBaK8KIdvGhRUgsv2sOLOng9ITfnq-vF2muqdHiaJ-ER6V1VFoggSuFjWMai2OSzMM9TlmQaYiSjc8a15kEK3iNWWWR4oOBvaibgOhU8JadlVZrnhGqttJ8nvlIh5zDVTrTieaaCSAVGBSKZknetIuV3R8YiYRKLKpegcokql1bl0BL1LNHyoEydNptN4HeQ70zOI4asRBD-TsnZqCWMrnp8urWUbJ7yg4QoWEDgLkI2JW-603glZiyWpqqhDe55j8NAzKbkmTNs1-eAWR486GU8MnnXADnfx2fK4pvlfo8Zx3jyxZ-79ZLc6x_DM3J63NfmFTk5ZPVri-Ff_L_Kgg |
link.rule.ids | 230,315,782,786,887,27933,27934 |
linkProvider | Flying Publisher |
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=High+expression+of+CDCA7+predicts+tumor+progression+and+poor+prognosis+in+human+colorectal+cancer&rft.jtitle=Molecular+medicine+reports&rft.au=Li%2C+Siman&rft.au=Huang%2C+Jiean&rft.au=Qin%2C+Mengbin&rft.au=Zhang%2C+Jinxiu&rft.date=2020-07-01&rft.pub=Spandidos+Publications+UK+Ltd&rft.issn=1791-2997&rft.eissn=1791-3004&rft.volume=22&rft.issue=1&rft.spage=57&rft.epage=66&rft_id=info:doi/10.3892%2Fmmr.2020.11089&rft.externalDBID=HAS_PDF_LINK |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1791-2997&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1791-2997&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1791-2997&client=summon |