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by
  • Wen Li1,2,†,
  • Shan-Shan Feng1,† and
  • Hao Wu2
  • et al.

Reviewer 1: Giovanni Vicidomini Reviewer 2: Anonymous

Round 1

Reviewer 1 Report

Authors present data on CDK1-related ceRNA network analysis from TCGA suggesting potential diagnostic biomarkers or therapeutic targets for lung adenocarcinoma treatment  from pathways related to LINC00460/LINC00525–hsa-mir-338–FAM111/ZWINT.

Methods and results are clear.

Language needs minor check and spelling check.

Some specific comments for section are listed below:

--Introduction needs to be improved, by adding more info on actual standard of care for lung cancer.

--Figure 1 shows descriptive data on CDK1 in TCGA. Is it possibile to summarize these data for better clarity in a summary table?

Some new analysis may help in improve the quality of data:

- Is it possible to add some data on correlation with EMT features?

- Data on immune infiltration are very interesting and promising. Can authors correlate these data with PD-L1 or immune scores available from literature for NSCLC? (see PMID: 32068166).

- Mutations of  FAM111B and ZWINT are presented. Is it possible to analyze the  co-mutations of these genes with other important genes related to LUAD  carcinogenesis (e.g. TP53, EGFR, KRAS)?

-- Discussion can also be improved by introducing some data on epithelial to emsenchymal transition as mechanism of resistance to theraphy in LUAD.

Author Response

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Author Response File: Author Response.docx

Reviewer 2 Report

The paper offers an interesting approach resulting in the construction of an axis that should be able to detect novel therapeutic targets.

Major issue: There is not enough clinical understanding of LUAD. LUAD is presented and discussed as a homogenous cancer. In reality prognosis of the disease is varying extremely depending on driver mutation or immunogenicity scored by PD-L1-IHC. The minimum approach to publish in a high-ranked journal would be to deliver full data on mutational status, PD-L1-expression, TMB plus clinical characteristics like smoking status.

 

minor: the role of EMT in the resistance of EGFR-mut tumours really play a minor role. Consider involving a clinician specialized in the treatment of lung cancer

Author Response

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Author Response File: Author Response.docx

Round 2

Reviewer 1 Report

Authors improved manuscript.

I would just suggest to remove oxalipatin from drugs cited in intro since it is not used worldwide for NSCLC.

Author Response

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Author Response File: Author Response.pdf

Reviewer 2 Report

Thank you very much for addressing my comments. Sorry to see that only a few driver mutations are included. 

Comment 2 was maybe misunderstood as it is not addressed in the answer. It was about the role of EMT in acquired EGFR-TKI-resistance

Author Response

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Author Response File: Author Response.pdf