2019
DOI: 10.1186/s12885-019-5952-2
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L1TD1 - a prognostic marker for colon cancer

Abstract: Background Prognostic markers specific to a particular cancer type can assist in the evaluation of survival probability of patients and help clinicians to assess the available treatment modalities. Methods Gene expression data was analyzed from three independent colon cancer microarray gene expression data sets ( N = 1052). Survival analysis was performed for the three data sets, stratified by the expression level of the LINE-1 type transposas… Show more

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Cited by 15 publications
(18 citation statements)
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“…These distinctive roles are dependent on its interaction partners. Several co-expression partners of L1TD1 already described in CRC have also been observed in our study, such as SPINK4, RETNLB, CLCA1, FcGBP, HEPACAM2, ITLN1 and , DEFA5 [ 42 ]. The common genes observed in our study with previous meta-analysis and other studies reinforces the importance of our findings.…”
Section: Discussionsupporting
confidence: 81%
“…These distinctive roles are dependent on its interaction partners. Several co-expression partners of L1TD1 already described in CRC have also been observed in our study, such as SPINK4, RETNLB, CLCA1, FcGBP, HEPACAM2, ITLN1 and , DEFA5 [ 42 ]. The common genes observed in our study with previous meta-analysis and other studies reinforces the importance of our findings.…”
Section: Discussionsupporting
confidence: 81%
“…In human embryonal stem cells, L1TD1 has also been associated with canonical markers of pluripotency that are also involved in cancerogenesis, such as OCT4 , NANOG , LIN28 and SOX2 [ 15 ]. With the use of bioinformatics analysis, a higher expression of L1TD1 in CRC was shown to be associated with longer disease-free survival [ 16 ]. Our results showed a positive trend of expression of L1TD1 to CRC cancerogenesis.…”
Section: Discussionmentioning
confidence: 99%
“…Moreover, in bladder cancer, it was suggested as a promising target for conjugate therapy [ 19 ]. A bioinformatics study on CRC showed differentially expressed SLITRK6 together with L1TD1 and ST6GALNAC1 [ 16 ], and it was downregulated in CRC compared to adenomas using microarray expression analysis [ 41 ]. However, our results showed no significant differences in expression between adenomas and CRC.…”
Section: Discussionmentioning
confidence: 99%
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