Method to detect prostate cancer in a sample

a prostate cancer and sample technology, applied in the field of prostate cancer, can solve the problems of only 79% of tpsa levels, unpredictability of prostate cancer screening psa, leakage of psa into blood, etc., and achieve the effect of facilitating the separation of bound target sequences

Inactive Publication Date: 2005-12-22
GEN PROBE INC
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0062] An “immobilized probe” or “immobilized nucleic acid” refers to a nucleic acid that joins, directly or indirectly, a capture oligomer to a solid support. An immobilized probe is an oligomer joined to a solid support that facilitates separation of bound target sequence from unbound material in a sample. Any known solid support may be used, such as matrices and particles free in solution, made of any known material (e.g., nitrocellulose, nylon, glass, polyacrylate,

Problems solved by technology

A number of conditions can result in leakage of PSA into the blood.
It is therefore not surprising that screening of serum PSA as an indicator of prostate cancer is not absolutely predictive.
However, the sensitivity of such elevated tPSA levels is only 79%; thus leaving 21% of patients with prostate cancer undetected.
The specificity for all tPSA values of 4 ng/ml or greater is very poor.
This low level of specificity results in additional more invasive and costly diagnostic procedures, such as transrectal ultrasounds and prostate biopsies.
Such tests when unnecessary are also very traumatic for the pati

Method used

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  • Method to detect prostate cancer in a sample
  • Method to detect prostate cancer in a sample
  • Method to detect prostate cancer in a sample

Examples

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example 1

CLINICAL PERFORMANCE USING ONE ILLUSTRATIVE EMBODIMENT OF THE METHODS OF THE PRESENT INVENTION

[0142] To estimate the clinical performance of the method, a pilot study was done on 517 patients planned to undergo ultrasound guided needle biopsies coming from five university medical centers located in Montreal and Quebec (Canada) between September 2001 and June 2002. Each sample was processed using the following steps:

Sample Collection

[0143] Following an attentive digital rectal examination, the first 20 to 30 ml of voided urine was collected in sterile 80 ml plastic containers (patient urinates directly in the sterile container).

[0144] An equal volume of Sample buffer (0.1M phosphate (0.06M Na2HPO4, 0.04M NaH2PO4) 0.3M NaCl, pH 7.0,) was immediately added and the solution mixed by inversion.

[0145] If not processed immediately, samples were refrigerated between 2-8° C. for up to three days until further processing. In view of the cell recovery step, freezing should be avoided.

C...

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Abstract

The present invention relates to prostate cancer. More specifically, the present invention relates to a method to detect prostate cancer in a patient sample by detecting the RNA encoded by the gene PCA3. More particularly the present invention relates to a method for determining a predisposition, or presence of prostate cancer in a patient comprising: (a) contacting a biological sample of a patient with at least one oligonucleotide that hybridizes to a PCA3 polynucleotide; (b) detecting in the biological sample an amount of PCA3 and second prostate specific polynucleotides; and (c) comparing the amount of PCA3 polynucleotide that hybridizes to the oligonucleotide to a predetermined cut off value, and therefrom determining the presence or absence of prostate cancer in the biological sample. The present invention further relates to diagnostic kits for the detection of prostate cancer or the risk of developing same in a patient comprising: (a) at least one container means having disposed therein at least one oligonucleotide probe or primer that hybridizes to one a PCA3 nucleic acid or complement thereof; (b) at least one oligonucleotide probe or primer that hybridizes with a second prostate specific nucleic acid or complement thereof; and (c) reagents enabling a detection of PCA3 and of the second prostate specific nucleic acid when PCA3 or second prostate-specific nucleic acid sequence is present.

Description

FIELD OF THE INVENTION [0001] The present invention relates to prostate cancer. More specifically, the present invention relates to a method to detect prostate cancer in a patient sample by detecting an RNA encoded by the prostate cancer antigen PCA3 gene. BACKGROUND OF THE INVENTION [0002] Over the last decade, cancer of the prostate has become the most commonly diagnosed malignancy among men and the second leading cause of male cancer deaths in the western population, following lung cancer. [0003] Early detection and treatment of prostate cancer before it has spread from the prostate gland, reduces the mortality of the disease. This is particularly true for younger men who are at greater risk of dying from this pernicious but slowly growing malignancy. This realization has prompted increasing efforts for early diagnosis and treatment. Indeed, the American Cancer Society and the American Urological Association recommend that male population at large undergo annual screening for pro...

Claims

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Application Information

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IPC IPC(8): C12Q1/68
CPCC12Q1/6886C12Q2600/16C12Q2600/158
Inventor FRADET, YVESCHYPRE, CAMILLEPICHE, LYSONGARON, GENEVIEVE
Owner GEN PROBE INC
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