TEST SYSTEM AND METHOD FOR DETECTING SESN1 GENE DELETIONS Russian patent published in 2022 - IPC C12Q1/68 G01N33/50 C12Q1/6886 

Abstract RU 2772504 C1

FIELD: medicine.

SUBSTANCE: invention relates to the field of medicine, oncology, in particular hematology. A pool of oligonucleotide primers has been proposed for the specific amplification of six microsatellite loci of SESN1 gene introns, which can be used in a test system for determining SESN1 gene deletions by multiplex polymerase chain reaction (PCR), as well as in a method for identifying patients with an unfavorable course of follicular lymphoma by the presence of significant SESN1 gene deletions using the aforementioned test system.

EFFECT: presence of deletions of the SESN1 gene in the case of heterozygous inheritance based on the absence of peaks of one of the alleles or a decrease in the intensity of its fluorescence relative to the peak of the second allele of the corresponding microsatellite locus in tumor tissue when compared with the control sample makes it possible to identify a group of patients with an unfavorable course of follicular lymphoma.

5 cl, 2 dwg, 1 tbl, 2 ex

Similar patents RU2772504C1

Title Year Author Number
TEST SYSTEM AND METHOD FOR DETECTING DELETIONS OF THE LONG ARM OF CHROMOSOME 6 2021
  • Sychevskaya Kseniya Andreevna
  • Kravchenko Sergej Kirillovich
  • Sudarikov Andrej Borisovich
RU2770892C1
SET OF STR-MARKERS OF THE Y-CHROMOSOME FOR DETERMINING THE ETHNO-TERRITORIAL ORIGIN OF AN INDIVIDUAL BASED ON A SAMPLE OF HIS DNA 2021
  • Stepanov Vadim Anatolevich
  • Kharkov Vladimir Nikolaevich
  • Kolesnikov Nikita Aleksandrovich
RU2804433C2
BIOMARKER PANEL AND METHODS FOR DETECTING MICROSATELLITE INSTABILITY IN VARIOUS TYPES OF CANCER 2019
  • De Craene, Bram
  • Decanniere, Klaas
  • Van De Velde, Jan
  • Maertens, Geert
RU2795410C2
GENETIC TEST FOR IDENTIFICATION OF RECESSIVE GENE CARRIER OF COMPLEX VERTEBRAL MALFORMATION IN CATTLE 2001
  • Bendiksen Khristian
  • Svendsen Sehren
  • Jansen Khelle
  • Panits Frank
  • Osberg Anders
  • Kholm Lars-Ehrik
  • Khorn Pehr
  • Khehj Anetta
  • Tomsen Bo
  • Jeppesen Mette
  • Nielsen Vivi Khunniske
  • Jonker Mark
RU2276690C2
TEST SYSTEM FOR DETERMINING IDH 1/2 GENE STATUS IN GLIAL TUMOR TISSUES 2023
  • Timoshkina Natalia Nikolaevna
  • Kutilin Denis Sergeevich
  • Gvaldin Dmitrii Iurevich
  • Novikova Inna Arnoldovna
  • Kavitskii Sergei Emmanuilovich
  • Rostorguev Eduard Evgenevich
RU2823028C1
METHOD FOR SEARCHING FOR ATP7B GENE MUTATIONS FOR DIAGNOSING WILSON'S DISEASE (WILSON-KONOVALOV) 2023
  • Garbuz Mikhail Maksimovich
  • Ovchinnikova Anna Aleksandrovna
  • Kumeiko Vadim Vladimirovich
RU2821573C1
OLIGONUCLEOTIDE SEQUENCE OLIGONUCLEOTIDE SEQUENCE FOR THE NRAS GENE Q61R MUTATION IN THE TUMOR FORMATIONS OF THE THYROID GLAND 2019
  • Kochergina-Nikitskaya Irina Nikolaevna
  • Vladimirova Ulyana Sergeevna
  • Rumyantsev Pavel Olegovich
RU2688189C1
MOLECULAR GENETIC SYSTEM FOR DETECTION OF DELETION SMN1 EXON 7 SUITABLE FOR NEONATAL SCREENING 2021
  • Polyakov Aleksandr Vladimirovich
  • Blagodatskikh Konstantin Aleksandrovich
  • Zabnenkova Viktoriya Vladimirovna
  • Kutsev Sergej Ivanovich
  • Shchagina Olga Anatolevna
  • Chausova Polina Aleksandrovna
  • Chukhrova Alena Lvovna
RU2796350C1
MINIMALLY INVASIVE METHOD FOR DIAGNOSIS OF HIGH-GRADE SEROUS OVARIAN ADENOCARCINOMA BASED ON COPY INDEX OF SULT1E1, CYP1B1, AND ESR1 GENES 2021
  • Kutilin Denis Sergeevich
  • Tsandekova Marietta Rafaelovn
  • Verenikina Ekaterina Vladimirovna
RU2750472C1
MINIMALLY INVASIVE METHOD FOR DETECTING SENSITIVITY OF RECTAL TUMOUR TO RADIATION THERAPY BASED ON CHANGE IN ABUNDANCE OF N2AX AND RBBP8 GENES 2019
  • Kutilin Denis Sergeevich
  • Kosheleva Nataliya Gennadevna
  • Gusareva Marina Aleksandrovna
  • Poluektov Sergej Igorevich
  • Legostaev Vladislav Mikhajlovich
  • Timoshkina Natalya Nikolaevna
  • Kit Oleg Ivanovich
RU2740576C1

RU 2 772 504 C1

Authors

Sychevskaya Kseniya Andreevna

Kravchenko Sergej Kirillovich

Sudarikov Andrej Borisovich

Dates

2022-05-23Published

2021-07-22Filed