Human RASSF1A/SHOX2 Gene Methylation Detection Kit
Mutiplex Fluorescence PCR
Human RASSF1A/SHOX2 Gene Methylation Detection Kit
Qualitative detection of SHOX2 and RASSF1 A double gene methylation in samples, for the auxiliary diagnosis of suspected lung cancer patients.
BACKGROUND

In 2022, the number of cancer deaths worldwide is estimated to be 9.7 million (including non-melanoma skin cancer). Among them, lung cancer is also the main cause of cancer death, with an estimated 1.8 million deaths, accounting for 18.7% of all cancer deaths[1].

The promoter regions of SHOX2 and RASSF1A in plasma samples of patients with lung cancer were found to be highly methylated. SHOX2, belonging to the SHOX gene family, plays a major role in the development of bone, heart, and nervous system during embryogenesis, and is abnormally expressed in lung cancer, breast cancer, and kidney cancer. The regulation of RASSF1A involves a variety of biological functions such as gene transcription, signal transduction, cell cycle, and apoptosis, and it can inhibit tumor formation through a variety of pathways.


BACKGROUND
DETECTION SIGNIFICANCE


Detection of methylation status of RASSF1A and SHOX2 genes in peripheral blood plasma can effectively improve the detection rate of early stage lung cancer and the survival rate of patients [3]. The early diagnosis of lung cancer is extremely important for the treatment of the disease. The earlier the diagnosis is confirmed, the better the prognosis will be and the longer the survival time will be. Screening is an important way to find lung cancer and precancerous lesions in the early stage.

 

References

[1] CA Cancer J Clin. 2024 May-Jun;74(3):229-263.

[2] Front Oncol. 2022 Jun 28; 12:849024.

[3] J Cancer Res Clin Oncol. 2020 Jun; 146(6):1379-1393


PRODUCT INFORMATION
Project Name
Core Technology
Pack Size
Instruments Validated
Sample Type
Human RASSF1A/SHOX2 Gene methylation detection kit
PAP-ARMS®
20 Tests / kit
ABI 7500, macro stone SLAN-96P/96S/48P, etc.
Peripheral blood
APPLICABLE PEOPLE

Long-term smoker

Early detection of small pulmonary nodules in patients with chronic pulmonary disease complicated with lung cancer: differentiation between benign and malignant

Early diagnosis of lung cancer in high risk group: blood lung cancer related tumor markers were positive

Patients with pleural effusion of unknown cause or patients with clinically high suspicion of tumors and unclear or negative morphological pathology

History of malignancy or family history of lung cancer

Occupational exposure history (asbestos, uranium and other contacts)

FEATURES & ADVANTAGES
Precise assistance

Precise assistance

cfDNA was extracted from peripheral blood plasma, and the double gene methylation in the samples was qualitatively detected. For the reference of auxiliary diagnosis for patients with suspected lung cancer, different typing and staging had high detection rate, and tumor progression could be evaluated vertically

Double target complementation

Double target complementation

methylation detection of SHOX2 and RASSF1A combined with double genes can complement each other and effectively improve the detection rate for patients with lung cancer

Sensitivity and specificity

Sensitivity and specificity

Compared with cytology and imaging detection, methylation detection is more stable and objective, making up for the deficiencies of sensitivity and imaging lag of cytology detection. Positive samples are not missed and negative samples are more reliable

Professional and efficient

Professional and efficient

Based on PAP-ARMS amplification technology with independent intellectual property right, the test can be completed in only one step, and the interpretation is simple and automatic reporting can be realized.

DETECTION PROCESS

1、Nucleic Acid Extraction

2、Set up qPCR

3、Amplification

4、Data Analysis