Lung cancer risk in germline p53 mutation carriers: association between an inherited cancer predisposition, cigarette smoking, and cancer risk.

Abstract:

:We recently observed a significantly increased risk for lung cancer in carriers of p53 germline mutations. Because cigarette smoking is known to play an important role in increasing the risk for lung cancer in the general population, we wanted to determine the role of cigarette smoking in lung cancer risk in people with a genetic susceptibility based on a p53 germline mutation. We studied 1263 people from 97 families enrolled in a cohort study of families systematically ascertained through childhood soft-tissue sarcoma patients treated at the M.D. Anderson Cancer Center, University of Texas, between 1944 and 1975. We assessed the incidence of lung and smoking-related cancers in 33 carriers of germline p53 mutations and in 1,230 noncarriers to determine whether there was an association between an inherited cancer predisposition, cigarette smoking, and cancer risk. We analyzed the association between cigarette smoking, mutation status, and lung and other smoking-related cancers by the Kaplan-Meier method and the Cox proportional hazards model with adjustments for birth year, race, and sex. In the hazards model, we incorporated a robust variance estimation to adjust for familial correlation. We observed an increased risk of a variety of histological types of lung cancer in the carriers of the p53 germline mutation. Mutation carriers who smoked had a 3.16-fold (95% confidence interval =1.48-6.78) higher risk for lung cancer than the mutation carriers who did not smoke. Our results demonstrate that cigarette smoking significantly increases lung cancer risk in carriers of a germline p53 mutation. This finding could be useful in designing strategies for early detection and treatment of lung and smoking-related cancers in individuals with this inherited cancer predisposition.

journal_name

Hum Genet

journal_title

Human genetics

authors

Hwang SJ,Cheng LS,Lozano G,Amos CI,Gu X,Strong LC

doi

10.1007/s00439-003-0968-7

keywords:

subject

Has Abstract

pub_date

2003-08-01 00:00:00

pages

238-43

issue

3

eissn

0340-6717

issn

1432-1203

journal_volume

113

pub_type

杂志文章
  • Pure gonadal dysgenesis (type XX). Report on a family with four affected sibs.

    abstract::A family with four 46,XX siblings affected by the pure gonadal dysgenesis syndrome is described. Inheritance is by an autosomal recessive gene limited to the female sex. ...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/BF00293782

    authors: Nazareth HR,Farah LM,Cunha AJ,Vieira FJ

    更新日期:1977-06-10 00:00:00

  • The mutational demography of protein C deficiency.

    abstract::The geographical distribution and prevalence of 256 single base-pair substitutions (105 of them being different) within the coding region of the human protein C (PROC) gene were correlated with their initial likelihoods of generation. A significant positive correlation was observed between these "mutational likelihood...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/BF00207369

    authors: Krawczak M,Reitsma PH,Cooper DN

    更新日期:1995-08-01 00:00:00

  • Alternative splicing in PAX2 generates a new reading frame and an extended conserved coding region at the carboxy terminus.

    abstract::PAX2 is a member of the PAX multigene family encoding transcription factors active in specific tissues during embryogenesis. Several PAX/Pax genes (PAX and Pax describe homologous genes in human and mice, respectively) have been shown to possess critical morphogenetic functions as identified by the analysis of mice ta...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/s004390050644

    authors: Tavassoli K,Rüger W,Horst J

    更新日期:1997-12-01 00:00:00

  • Mapping of the kinesin-related gene ATSV to chromosome 2q37.

    abstract::The human ATSV (axonal transporter of synaptic vesicles) gene encodes an anterograde axonal motor transport protein and demonstrates homology to the kinesin gene family in several species. The human ATSV gene was mapped to chromosome 2q37 by screening of a human/rodent somatic cell hybrid panel by the polymerase chain...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/s004390050944

    authors: Keller MP,Seifried BA,Rabin BA,Chance PF

    更新日期:1999-03-01 00:00:00

  • A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss.

    abstract::Usher syndrome is an autosomal recessive condition characterized by sensorineural hearing loss, variable vestibular dysfunction, and visual impairment due to retinitis pigmentosa (RP). The seven proteins that have been identified for Usher syndrome type 1 (USH1) and type 2 (USH2) may interact in a large protein comple...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/s00439-006-0304-0

    authors: Ebermann I,Scholl HP,Charbel Issa P,Becirovic E,Lamprecht J,Jurklies B,Millán JM,Aller E,Mitter D,Bolz H

    更新日期:2007-04-01 00:00:00

  • Molecular characterization of a ring X chromosome in a male with short stature.

    abstract::We report the molecular characterization of a ring X chromosome that was transmitted from a mother to a male who has short stature and minor dysmorphic features. This represents only the second reported ring X chromosome in a male. The ring is derived from breakage within the Xp pseudoautosomal region (PAR) and just p...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/s00439-002-0685-7

    authors: Ellison JW,Tekin M,Sikes KS,Yankowitz J,Shapiro L,Rappold GA,Neely KE

    更新日期:2002-04-01 00:00:00

  • Assignment of human plasma methylumbelliferyl-tetra-N-acetylchitotetraoside hydrolase or chitinase to chromosome 1q by a linkage study.

    abstract::Plasma methylumbelliferyl tetra-N-acetylchitotetraoside hydrolase or chitinase (CHIT) might play a role in degrading the chitin wall of some microorganisms. In about 6% of Caucasian people the enzyme shows pseudodeficiency (defined as very low activity without apparent symptoms). We have mapped this locus by linkage a...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/s004390050615

    authors: Eiberg H,Den Tandt WR

    更新日期:1997-12-01 00:00:00

  • In-frame deletions of BRCA1 may define critical functional domains.

    abstract::The identification of genomic rearrangements involving more than 0.5 kb of the BRCA1 gene has confirmed a more complex mutation spectrum than was initially appreciated. Genomic rearrangements in BRCA1 represent 15% of all mutations in a group of French and American breast and ovarian cancer families and 36% of all mut...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/s004390000372

    authors: Rohlfs EM,Chung CH,Yang Q,Skrzynia C,Grody WW,Graham ML,Silverman LM

    更新日期:2000-10-01 00:00:00

  • Distribution of Gd- alleles in some ethnic groups of the USSR.

    abstract::A population study of Gd- allele distribution was made in similar (age-sex) samples of schoolchildren and students from different ethnic groups: Russians, Ashkenazi Jews, and Azerbaijanians. Both the frequency and the spectrum of the Gd- alleles were quite different. The Gd- frequency in Russians (Kostroma region) was...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/BF00281070

    authors: Krasnopolskaya XD,Shatskaya TL

    更新日期:1987-03-01 00:00:00

  • Plasminogen with type-I mutation is polymorphic in the Japanese population.

    abstract::A functionally inactive plasminogen (PLG) variant designated as PLG M5 is polymorphic in the Japanese population and has a feature common to PLG with type-I mutation that has a codon 601 missense mutation in exon 15 (GCT for Ala-->ACT for Thr). This study was conducted to clarify whether the type-I mutation of PLG is ...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/BF00210737

    authors: Kikuchi S,Yamanouchi Y,Li L,Kobayashi K,Ijima H,Miyazaki R,Tsuchiya S,Hamaguchi H

    更新日期:1992-09-01 00:00:00

  • X-linked steroid sulfatase: evidence for different gene-dosage in males and females.

    abstract::Steroid sulfatase (STS) activities in female fibroblast strains are significantly higher than in male strains, as determined by cleavage of dehydroepiandrosterone sulfate. The difference is probably not due to hormonal control of gene expression, but suggests that for this X-linked locus there is no gene dosage compen...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/BF00278971

    authors: Müller CR,Migl B,Traupe H,Ropers HH

    更新日期:1980-01-01 00:00:00

  • ELMOD3, a novel causative gene, associated with human autosomal dominant nonsyndromic and progressive hearing loss.

    abstract::Autosomal dominant nonsyndromic hearing loss (ADNSHL) is a highly genetically heterogeneous disorder. Up to date only approximately 37 ADNSHL-causing genes have been identified. The goal of this study was to determine the causative gene in a five-generation Chinese family with ADNSHL. A Chinese family was ascertained....

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/s00439-018-1885-0

    authors: Li W,Sun J,Ling J,Li J,He C,Liu Y,Chen H,Men M,Niu Z,Deng Y,Li M,Li T,Wen J,Sang S,Li H,Wan Z,Richard EM,Chapagain P,Yan D,Liu XZ,Mei L,Feng Y

    更新日期:2018-04-01 00:00:00

  • Parental age and seasonal variation in the births of children with sporadic retinoblastoma: a mutation-epidemiologic study.

    abstract::Statistical analysis of parental age data from 225 sporadic cases of bilateral retinoblastoma, plus ten sporadic cases of chromosome deletion or translocation involving 13q14 that was identified as of paternal origin, revealed no evidence of paternal or maternal age effect. Parental exposure to ionizing radiation or c...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/BF00208931

    authors: Matsunaga E,Minoda K,Sasaki MS

    更新日期:1990-01-01 00:00:00

  • Hemoglobin G San José [beta 2 7 (A4) Glu to Gly alpha 2], beta thalassemia, and alpha thalassemia in a Sicilian family.

    abstract::A 3-year-old child of Sicilian origin was found to have a severe form of Cooley's anemia. Investigations were extended to other members of her family. In three, a rare beta-chain structural Hb variant, Hb G San José [beta 7 (A4) Glu to Gly], was observed: in the father of the porposita heterozygosity for the abnormal ...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/BF00271579

    authors: Musumeci S,Schilirò G,Pizzarelli G,Tentori L,Marinucci M,Fontanarosa PP,Russo G

    更新日期:1979-11-01 00:00:00

  • Peculiarities of the GSTM1 0/0 genotype in French heavy smokers with various types of chronic bronchitis.

    abstract::A homozygous gene deletion of the glutathione S-transferase M1 (GSTM1) locus of genomic DNA from blood spots was studied by the polymerase chain reaction in a group of French heavy smokers (n = 361), which included patients with severe chronic bronchitis (SCB; n = 87), moderate chronic bronchitis (MCB: n = 102) and ha...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/s004390050455

    authors: Baranova H,Perriot J,Albuisson E,Ivaschenko T,Baranov VS,Hemery B,Mouraire P,Riol N,Malet P

    更新日期:1997-06-01 00:00:00

  • Amplified product length polymorphism (APLP): a novel strategy for genotyping the ABO blood group.

    abstract::We present a simple rapid reproducible polymerase chain reaction based technique, termed amplified product length polymorphism (APLP), as a new strategy for primer design for ABO genotyping. The method involves the use of primers differing in length and permits the identification of the major ABO genotypes (A1, A2, B,...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/s004390050306

    authors: Watanabe G,Umetsu K,Yuasa I,Suzuki T

    更新日期:1997-01-01 00:00:00

  • Meiotic arrest at first spermatocyte level: a new inherited infertility disorder.

    abstract::Three 46,XY phenotypically male, azoospermic brothers out of thirteen sibs from a consanguineous marriage were studied and found to have a unique pattern of testicular histology with arrest of spermatogenesis at the pachytene stage of primary spermatocytes. Endocrinological evaluation showed elevated plasma luteinizin...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/BF00295476

    authors: Cantú JM,Rivas F,Hernández-Jáuregui P,Díaz M,Cortés-Gallegos V,Vaca G,Velázquez A,Ibarra B

    更新日期:1981-01-01 00:00:00

  • Four new haplotypes observed in Algerian beta-thalassemia patients.

    abstract::beta-Thalassemia, a heterogeneous group of human anemias affecting the expression of beta-globin, is caused by a number of molecular defects. Restriction endonuclease mapping of ethnic populations has revealed many polymorphisms within and around the beta-like globin genes, combinations of which are assigned as haplot...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/BF00286665

    authors: Beldjord C,Lapouméroulie C,Baird ML,Girot R,Adjrad L,Lenoir G,Benabadji M,Labie D

    更新日期:1983-01-01 00:00:00

  • A sterile male with 45,X0 and a Y;22 translocation.

    abstract::Cytogenetic analysis of a 20-year-old sterile male revealed a 45,X0 karyotype with no evidence for Y-chromosomal material on any of the chromosomes analysed by Q-, G- and C-banding. DNA analysis with 17 different Y chromosome-derived probes revealed the presence of Yp DNA sequences in the patient's genome. In situ hyb...

    journal_title:Human genetics

    pub_type: 杂志文章,评审

    doi:10.1007/BF00204168

    authors: Arnemann J,Schnittger S,Hinkel GK,Tolkendorf E,Schmidtke J,Hansmann I

    更新日期:1991-06-01 00:00:00

  • Extensive analysis of 40 infertile patients with congenital absence of the vas deferens: in 50% of cases only one CFTR allele could be detected.

    abstract::Mutations in the cystic fibrosis (CF) conductance transmembrane regulator (CFTR) gene have been detected in patients with CF and in males with infertility attributable to congenital bilateral absence of the vas deferens (CBAVD). Thirty individuals with CBAVD and 10 with congenital unilateral absence of the vas deferen...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/BF00209403

    authors: Casals T,Bassas L,Ruiz-Romero J,Chillón M,Giménez J,Ramos MD,Tapia G,Narváez H,Nunes V,Estivill X

    更新日期:1995-02-01 00:00:00

  • Acceptability of carrier screening for cystic fibrosis during pregnancy in a German population.

    abstract::A pilot project offering voluntary heterozygote screening for the delta F508 mutation causing cystic fibrosis (CF) to 638 pregnant women attending two antenatal clinics in the eastern part of Berlin was carried out from 1990-1993. Participation was invited using an information leaflet and inclusion in the study was co...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/BF02272835

    authors: Jung U,Urner U,Grade K,Coutelle C

    更新日期:1994-07-01 00:00:00

  • Genetic variants in components of the NALCN-UNC80-UNC79 ion channel complex cause a broad clinical phenotype (NALCN channelopathies).

    abstract::NALCN is a conserved cation channel, which conducts a permanent sodium leak current and regulates resting membrane potential and neuronal excitability. It is part of a large ion channel complex, the "NALCN channelosome", consisting of multiple proteins including UNC80 and UNC79. The predominant neuronal expression pat...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/s00439-018-1929-5

    authors: Bramswig NC,Bertoli-Avella AM,Albrecht B,Al Aqeel AI,Alhashem A,Al-Sannaa N,Bah M,Bröhl K,Depienne C,Dorison N,Doummar D,Ehmke N,Elbendary HM,Gorokhova S,Héron D,Horn D,James K,Keren B,Kuechler A,Ismail S,Issa MY

    更新日期:2018-09-01 00:00:00

  • A 5'-truncated c-myc gene variant not associated with a risk of cancer.

    abstract::By analyzing c-myc specific fragments from white blood cell DNAs of 98 gastric cancer patients and 46 control subjects, we observed 6 unexpected patterns due to presence of a variant c-myc gene in addition to the normal gene. Restriction enzyme mapping indicated that the variant c-myc gene was the result of a 5' delet...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/BF00209016

    authors: Pellegata NS,Bergamaschi G,Amadori D,Aloia A,Ballarini P,Del Senno L,Amaducci L,Ranzani GN

    更新日期:1991-09-01 00:00:00

  • Autosomal dominant polycystic kidney disease: evidence for the existence of a third locus in a Portuguese family.

    abstract::Autosomal dominant polycystic kidney disease is characterized by clinical and genetic heterogeneity. Two loci implicated in the disease have previously been mapped (PKD1 on chromosome 16 and PKD2 on chromosome 4). By two point and multipoint linkage analysis, negative lod scores have been found for both chromosome 16 ...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/BF00214191

    authors: de Almeida S,de Almeida E,Peters D,Pinto JR,Távora I,Lavinha J,Breuning M,Prata MM

    更新日期:1995-07-01 00:00:00

  • Generation or birth cohort effect on cancer risk in Li-Fraumeni syndrome.

    abstract::Genetic anticipation is the increased incidence, earlier onset, or increased severity of a disease in successive generations. Before the biological basis of anticipation had been demonstrated, the phenomenon was thought to be due to sampling bias, epigenetic effects, gene conversion, or recombinant events. Since then,...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/s00439-005-0016-x

    authors: Brown BW,Costello TJ,Hwang SJ,Strong LC

    更新日期:2005-12-01 00:00:00

  • A unique genome-wide association analysis in extended Utah high-risk pedigrees identifies a novel melanoma risk variant on chromosome arm 10q.

    abstract::Only two genome-wide association (GWA) screens have been published for melanoma (Nat Genet 47:920-925, 2009; Nat Genet 40:838-840, 2008). Using a unique approach, we performed a genome-wide association study in 156 related melanoma cases from 34 high-risk Utah pedigrees. Genome-wide association analysis was performed ...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/s00439-011-1048-z

    authors: Teerlink C,Farnham J,Allen-Brady K,Camp NJ,Thomas A,Leachman S,Cannon-Albright L

    更新日期:2012-01-01 00:00:00

  • Deficiency, transposition, and duplication of one 15q region may be alternatively associated with Prader-Willi (or a similar) syndrome. Analysis of seven cases after varying ascertainment.

    abstract::Seven patients are described who have some or all of the symptoms of Prader-Willi syndrome. They were ascertained by varying criteria starting either from the clinical picture or from the identification of a chromosome abnormality involving the proximal portion of the long arm of chromosome 15. The chromosome abnormal...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/BF00292373

    authors: Fraccaro M,Zuffardi O,Bühler E,Schinzel A,Simoni G,Witkowski R,Bonifaci E,Caufin D,Cignacco G,Delendi N

    更新日期:1983-01-01 00:00:00

  • Exhaustive screening of the 21-hydroxylase gene in a population of hyperandrogenic women.

    abstract::21-hydroxylase (21-OH) deficiency accounts for the vast majority of nonclassic (NC) forms of congenital adrenal hyperplasia (CAH), and is associated with symptoms detectable either in childhood (precocious puberty) or sometimes only later in adulthood (hirsutism, acne, amenorrhea). While the severe forms of the diseas...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/s004390050586

    authors: Blanché H,Vexiau P,Clauin S,Le Gall I,Fiet J,Mornet E,Dausset J,Bellanné-Chantelot C

    更新日期:1997-11-01 00:00:00

  • RFLP haplotyping and mutation analysis of the phenylalanine hydroxylase gene in Dutch phenylketonuria families.

    abstract::Restriction fragment length polymorphism haplotyping of mutated and normal phenylalanine hydroxylase (PAH) alleles in 49 Dutch phenylketonuria (PKU) families was performed. All mutant PAH chromosomes identified by haplotyping (n = 98) were screened for eight of the most predominant mutations. Compound heterozygosity w...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/BF00420944

    authors: Meijer H,Jongbloed RJ,Hekking M,Spaapen LJ,Geraedts JP

    更新日期:1993-12-01 00:00:00

  • Genome scans and gene expression microarrays converge to identify gene regulatory loci relevant in schizophrenia.

    abstract::Multiple linkage regions have been reported in schizophrenia, and some appear to harbor susceptibility genes that are differentially expressed in postmortem brain tissue derived from unrelated individuals. We combined traditional genome-wide linkage analysis in a multiplex family with lymphocytic genome-wide expressio...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/s00439-006-0172-7

    authors: Vawter MP,Atz ME,Rollins BL,Cooper-Casey KM,Shao L,Byerley WF

    更新日期:2006-06-01 00:00:00