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by
  • Francesca Megiorni1,*,
  • Simona Camero2 and
  • Paola Pontecorvi1
  • et al.

Reviewer 1: Anonymous Reviewer 2: Anonymous Reviewer 3: Anonymous

Round 1

Reviewer 1 Report

This study deals with the effect of OTX-015 on ovarian carcinoma cell lines. There are several points to be addressed further.

#1. In Fig. 3d, the decrease of colony-forming capacity of tumor cells is not evident. A colony-forming assay or limiting dilution assay should be supplemented.

#2. In Fig. 5d, the combination has more effect than IR alone, but it is not clear that OTX-015 and IR have a true synergistic effect. OTX-015 alone seems to result in the similar outcome. Is there any evidence of radio-sensitization of OTX-015?

#3. The first line treatment for ovarian cancer is the combination of cisplatin and paclitaxel. The effect of any novel agent needs to be compared with the standard.

#4. OTX-015 is known as an epigenetic regulator. Is there any proof that wide-spread changes of epigenetic modulation take place after drug treatment? Only decrease of BRD4 expression is too weak to demonstrate the mechanism.

#5. No in vivo experiment is done. The effect of OTX-015 requires to be verified in animal models of ovarian cancer.

Author Response

Please see the attachment.

Author Response File: Author Response.pdf

Reviewer 2 Report

THE CONTRIBUTION IS VERY INTERESTING EVEN MORE THAN 20 PAGES

Author Response

Please see the attachment.

Author Response File: Author Response.pdf

Reviewer 3 Report

Thank you for allowing me to review this interesting manuscript.

The paper is well written

The topic is innovative, acutally I have not major comment

 

Just a minor commnet

Is there a correlation between OTX015 and BRCA status?

 

 

 

Author Response

Please see the attachment.

Author Response File: Author Response.pdf