Can PCR detect chromosomal translocations in cancer?

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Discussion Overview

The discussion centers on the ability of PCR (Polymerase Chain Reaction) to detect chromosomal translocations associated with cancer, specifically focusing on the BCR-ABL1 fusion gene in leukemias. Participants explore the methodologies involved, including conventional PCR and RT-PCR, and the implications of using each technique for detection.

Discussion Character

  • Technical explanation
  • Debate/contested

Main Points Raised

  • Some participants explain that PCR can detect specific chromosomal translocations, such as the BCR-ABL1 fusion, by using primers that target the genes involved in the translocation.
  • Others clarify that RT-PCR involves reverse transcribing RNA into cDNA before amplification, suggesting it may be relevant for detecting the BCR-ABL1 mRNA.
  • One participant questions whether finding BCR-ABL mRNA would be easier than detecting the fused DNA, indicating a lack of consensus on the preferred method.
  • Some participants note that conventional PCR is typically used to look for chromosomal translocations at the DNA level, while others mention that RT-qPCR is commonly employed for diagnosis.
  • There is a discussion about the stability of DNA versus RNA, with some suggesting that DNA might be preferable for detection due to its stability.

Areas of Agreement / Disagreement

Participants express differing views on the methods used for detecting the BCR-ABL1 fusion gene, with some advocating for conventional PCR and others for RT-PCR. The discussion remains unresolved regarding which method is definitively preferred for this purpose.

Contextual Notes

Participants reference specific studies and articles to support their claims, indicating that the discussion is informed by existing literature, but there are still uncertainties regarding the methodologies and their effectiveness.

TytoAlba95
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How is PCR able to detect chromosomal translocations causing cancer?

I understand it is possible through FISH but how PCR?
 
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Hi SanjuktaGhosh.

I think they are referring to RT-PCR. Both PCR and RT-PCR involve making copies of DNA but in RT-PCR one first uses reverse transcriptase to reverse transcribe a subject RNA strand into its DNA complement (cDNA). One then uses PCR to amplify the cDNA.

AM
 
PCR is able to detect specific chromosomal translocations, such as the "Philadelphia chromosome" that produces the BCR-ABL1 fusion in many leukemias. Basically, since the genes for BCR and ABL1 are normally on different chromosomes, a PCR reaction using one primer against BCR and one primer against ABL1 will normally not produce a product. However, if a translocation has occurred which creates the BCR-ABL1 fusion, the PCR reaction will then amplify the BCR-ABL1 gene, enabling detection of the fusion. PCR methods are very sensitive, allowing researchers to detect minute amounts of fused DNA in a mixed population of normal and cancerous cells.

https://www.lls.org/leukemia/chronic-myeloid-leukemia/diagnosis
https://www.cancer.org/cancer/chron...etection-diagnosis-staging/how-diagnosed.html

Andrew Mason said:
I think they are referring to RT-PCR. Both PCR and RT-PCR involve making copies of DNA but in RT-PCR one first uses reverse transcriptase to reverse transcribe a subject RNA strand into its DNA complement (cDNA). One then uses PCR to amplify the cDNA.

No, these tests are normally done by conventional PCR, looking for chromosomal translocations at the DNA level.
 
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Ygggdrasil said:
No, these tests are normally done by conventional PCR, looking for chromosomal translocations at the DNA level.
Would finding the BCR-ABL mRNA be easier than finding the fused DNA? This is not my area, but RT-PCR does seem to be used for this purpose: See for example: https://www.ncbi.nlm.nih.gov/pubmed/17705578

AM
 
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Andrew Mason said:
Would finding the BCR-ABL mRNA be easier than finding the fused DNA? This is not my area, but RT-PCR does seem to be used for this purpose: See for example: https://www.ncbi.nlm.nih.gov/pubmed/17705578

AM

Typically, DNA is more stable than RNA, so I would have thought that it would be preferable to check DNA by qPCR. Upon further investigation, it does appear that you are correct and diagnosis is typically done by RT-qPCR to look for BCR-ABL1 mRNA (e.g. see http://www.bloodjournal.org/content/114/5/937.long?sso-checked=true).
 
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Thank you both of you. So basically to detect BCR-ABL1 fusion gene, a forward primer that anneals to the starting portion of BCR and a reverse primer that anneals to the ending portion of ABL1 are used?
 

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