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Review
Peer-Review Record

Molecular Genetics in Neuroblastoma Prognosis

Children 2021, 8(6), 456; https://doi.org/10.3390/children8060456
by Margherita Lerone 1, Marzia Ognibene 1, Annalisa Pezzolo 2, Giuseppe Martucciello 3,4, Federico Zara 1,4, Martina Morini 5,*,† and Katia Mazzocco 6,†
Reviewer 1: Anonymous
Reviewer 2:
Children 2021, 8(6), 456; https://doi.org/10.3390/children8060456
Submission received: 20 April 2021 / Revised: 23 May 2021 / Accepted: 27 May 2021 / Published: 29 May 2021
(This article belongs to the Section Pediatric Surgery)

Round 1

Reviewer 1 Report

The present Review article reports about actual state of molecular genetics in neuroblastoma, focused on prognostic impact.

It is a very well written overview about molecular genetics in neuroblastoma.

The paper is well organized and profound review of actual literature is clearly visible.

The abstract is short and on the point clear and invites to read the whole paper.

Introduction is leading to the purpose of the review - reporting the genetic implications in the pathogenesis of neuroblastoma.

The main chapter, devided in»First evidences of genetics in NB» and «Brand new emerging genetic implications in NB» shows in a dynamic matter the recent development in research on this topic. It provides an excellent overview for interested physicians and researcher, in a broad understandable manner.

Conclusions are as clear as possible and next to the general aspect, as usually in reviews, there is an outview in direction of targeted therapies in the sense of translational research and results of scientific workup.

 

Author Response

Please see the attachment

Author Response File: Author Response.docx

Reviewer 2 Report

This review is well-written but the similar reviews have already published. `In recent standpoint, telomere maintenance is suggested as a "driver " of unfavorable NB. The segmental chromosome aberration might be the result of chromosome instability due to telomere crisis. After telomere crisis, telomerase activation of ALT occur in unfavorable  NB. Therefore, the authors should be the correlation among these genetic aberrations.

Author Response

Please see the attachment

Author Response File: Author Response.docx

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