Evidence map›Paper›PMID 24575188›Full record

ArticleTropical life sciences research2010

Identification of Chromosomal Aberrations by Using Trypsin G-banding in Hepatocellular Carcinoma Patients (HCC) in Tamil Nadu, India.

Subramaniam Mohana Devi, Vellingiri Balachandar, Palanivel Vel Murugan, Keshavarao Sasikala, Pappusamy Manikantan, Leela Krishnan Venkatakrishnan

Open access · greenAbstract read
In one paragraph

Article in Tropical life sciences research, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 41% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 2 countries.

Subramaniam Mohana DeviHuman Genetics Laboratory, Department of Zoology, School of Life Science, Bharathiar University, Coimbatore-641046, Tamil Nadu, India.
Vellingiri BalachandarHuman Genetics Laboratory, Department of Zoology, School of Life Science, Bharathiar University, Coimbatore-641046, Tamil Nadu, India.
Palanivel Vel MuruganDivision of Biotechnology, College of Environmental and Bioresource Sciences, Chonbuk National University, South Korea.
Keshavarao SasikalaHuman Genetics Laboratory, Department of Zoology, School of Life Science, Bharathiar University, Coimbatore-641046, Tamil Nadu, India.
Pappusamy ManikantanHuman Genetics Laboratory, Department of Zoology, School of Life Science, Bharathiar University, Coimbatore-641046, Tamil Nadu, India.
Leela Krishnan VenkatakrishnanDepartment of Gastroenterology, PSG Hospital, Coimbatore, Tamil Nadu, India.
Jeonbuk National University · KRKG Hospital · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) (or liver cancer) is one of the most common human malignancies worldwide. Aetiologically, HCC is closely associated with chronic hepatitis B and C virus infection, cirrhosis and alcohol intake. The objective of the present study was to elucidate the chromosomal abberations (CA) in HCC patients using the trypsin G-banding technique. This study may help in understanding the pattern of the disease and to assess whether these aberrations are associated with HCC susceptibility. The study examined 51 HCC cases and an equal number (n = 51) of age and gender matched cancer-free controls recruited from the hospitals in Tamil Nadu. The HCC cases were grouped depending upon their age into group I (≤ 45 years) and group II (≥ 46 years). The development of effective markers for the detection of HCC could have an impact on cancer mortality and may have significant public health implications worldwide. Subjects were recruited based on their alpha-fetoprotein (AFP) serum level, which is an effective marker for HCC. In the HCC cases, a higher number of chromatid aberrations [group I 13(25.5%) and group II 43(84.3%)] and CA [group I 10(19.6%) and group II 28(54.9%)] were observed. In contrast, controls showed a lower number of chromatid [group I 5(9.8%) and group II 12(23.5%)] and CA [group I 4(7.8%) and group II 9(17.6%)]. In conclusion, the results of this study contribute to the validation of CA as an intermediate end point in carcinogenesis. Because many people are unaware of this lethal disease, this study will raise awareness of this cancer.

Indexed as

Alpha-fetoprotein (AFP)Chromosomal aberrations (CA)CytogeneticsHepatocellular Carcinoma (HCC)

Identifiers

PMID24575188
PMCPMC3819068
OpenAlexW1887225317

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.