Can PCR detect chromosomal translocations in cancer?

In summary, PCR methods, specifically RT-PCR, are able to detect chromosomal translocations causing cancer, such as the BCR-ABL1 fusion. This is achieved by using primers that target specific genes and amplifying them through PCR, allowing for the detection of fused DNA in a mixed population of normal and cancerous cells. While conventional PCR is normally used, some studies have also utilized RT-PCR for this purpose.
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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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  • #2
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
 
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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?
 

FAQ: Can PCR detect chromosomal translocations in cancer?

1. What is PCR and how is it used in cancer detection?

PCR (polymerase chain reaction) is a laboratory technique used to amplify a specific DNA sequence. In cancer detection, PCR is used to identify and amplify cancer-related DNA or RNA markers, such as mutations or gene expression levels, in a small sample of tissue or body fluid.

2. How accurate is PCR in detecting cancer?

PCR is a highly sensitive and specific technique, meaning it can accurately detect even small amounts of cancer-related DNA or RNA markers. However, the accuracy of the results depends on the quality and quantity of the sample, as well as the expertise of the lab performing the test.

3. What types of cancer can be detected using PCR?

PCR can be used to detect a wide range of cancers, including solid tumors and blood-related cancers. It can also be used to detect specific types of cancer, such as breast cancer or lung cancer, by targeting specific DNA or RNA markers associated with those cancers.

4. How is PCR used in cancer diagnosis and treatment?

PCR can be used in cancer diagnosis to confirm the presence of cancer and determine its type and stage. It can also be used to monitor the effectiveness of cancer treatment by tracking changes in cancer-related DNA or RNA markers over time. Additionally, PCR can be used in research to identify potential new biomarkers for cancer detection or to develop personalized treatment plans.

5. Are there any limitations or drawbacks to using PCR in cancer detection?

While PCR is a powerful tool in cancer detection, there are some limitations and drawbacks to consider. It requires specialized equipment and trained personnel to perform, which can be costly and time-consuming. Additionally, PCR can only detect known DNA or RNA markers, so it may miss rare or unknown mutations. Finally, false positives or false negatives can occur if the sample is contaminated or if there are errors in the testing process.

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